The following data is part of a premarket notification filed by Medical Insights, Inc. with the FDA for Kittner Dissector/peanut/cherry/stick/triangle Sponge/gauze Rosebud.
Device ID | K940904 |
510k Number | K940904 |
Device Name: | KITTNER DISSECTOR/PEANUT/CHERRY/STICK/TRIANGLE SPONGE/GAUZE ROSEBUD |
Classification | Gauze/sponge, Internal |
Applicant | MEDICAL INSIGHTS, INC. 193 WHITEHALL AVE. Mystic, CT 06355 |
Contact | Robert J Caricato |
Correspondent | Robert J Caricato MEDICAL INSIGHTS, INC. 193 WHITEHALL AVE. Mystic, CT 06355 |
Product Code | EFQ |
CFR Regulation Number | 510(k) Premarket Notification [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-02-24 |
Decision Date | 1994-04-14 |