3-WAY STOPCOCK
Stopcock, I.v. Set
MEDEX, INC.
The following data is part of a premarket notification filed by Medex, Inc. with the FDA for 3-way Stopcock.
Pre-market Notification Details
Device ID | K782168 |
510k Number | K782168 |
Device Name: | 3-WAY STOPCOCK |
Classification | Stopcock, I.v. Set |
Applicant | MEDEX, INC. 4221 Richmond Rd., N.W. Walker, MI 49534 |
Product Code | FMG |
CFR Regulation Number | 880.5440 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1978-12-29 |
Decision Date | 1979-02-22 |
NIH GUDID Devices
Device Identifier | submissionNumber | Supplement |
50351688505369 |
K782168 |
000 |
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