Network Eye Spears, Points, Drains, Wicks And Shields 510(k) FDA Premarket Notification K130117 NETWORK MEDICAL PRODUCTS, LTD.

Pre-market Notification Details

Device ID	K130117
510k Number	K130117
Device Name:	NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDS
Classification	Sponge, Ophthalmic
Applicant	NETWORK MEDICAL PRODUCTS, LTD. Coronet House, Kearsley Road Ripon, GB Hg4 2sg
Contact	Alison March
Correspondent	Alison March NETWORK MEDICAL PRODUCTS, LTD. Coronet House, Kearsley Road Ripon, GB Hg4 2sg
Product Code	HOZ
CFR Regulation Number	886.4790 [🔎]
Decision	Substantially Equivalent (SESE)
Type	Traditional
3rd Party Reviewed	No
Combination Product	No
Date Received	2013-01-16
Decision Date	2013-10-29
Summary:	summary

NIH GUDID Devices

Device Identifier	submissionNumber	Supplement
05060165012466	K130117	000
05056100707511	K130117	000
05056100707504	K130117	000
05056100707474	K130117	000
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05060165014224	K130117	000
05060165013906	K130117	000
05060165012480	K130117	000

NETWORK EYE SPEARS, POINTS, DRAINS, WICKS AND SHIELDS

Sponge, Ophthalmic

NETWORK MEDICAL PRODUCTS, LTD.

Pre-market Notification Details

NIH GUDID Devices