acculove

GUDID 00854314007206

Famidoc Technology Co.,Ltd.

Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system Physical therapy transcutaneous neuromuscular electrical stimulation system

Primary Device ID	00854314007206
NIH Device Record Key	f52d6007-781a-4c8d-864f-e71e438c2db1
Commercial Distribution Status	In Commercial Distribution
Brand Name	acculove
Version Model Number	FDES116
Company DUNS	421343701
Company Name	Famidoc Technology Co.,Ltd.
Device Count	1
DM Exempt	false
Pre-market Exempt	false
MRI Safety Status	Labeling does not contain MRI Safety Information
Human Cell/Tissue Product	false
Device Kit	false
Device Combination Product	false
Single Use	false
Lot Batch	true
Serial Number	false
Manufacturing Date	false
Expiration Date	false
Donation Id Number	false
Contains Natural Rubber Latex	false
Labeled No Natural Rubber Latex	false
RX Perscription	true
OTC Over-The-Counter	false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00854314007206 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

Premarket Notification: K130723

FDA Product Code

GZJ	Stimulator, Nerve, Transcutaneous, For Pain Relief

Sterilization

Steralize Prior To Use	false
Device Is Sterile	false

Device Entry Metadata

Public Version Status	Update
Device Record Status	Published
Public Version Number	2
Public Version Date	2019-10-23
Device Publish Date	2019-09-29

On-Brand Devices [acculove]

00854314007237	FDES108
00854314007220	FDES116
00854314007190	FDIR-V4
00854314007183	The product is suitable to be used for temporary relief of pain associated with sore and aching
00854314007206	FDES116
00818218024813	FDES108
00818218024806	FDES116
00818218024790	FDES116
00818218021058	FDIR-V4
00818218029047	The product is suitable to be used for temporary relief of pain associated with sore and aching

Trademark Results [acculove]

Mark Image Registration \| Serial	Company Trademark Application Date
ACCULOVE 88091139 not registered Live/Pending	Cao liang 2018-08-24