The following data is part of a premarket notification filed by Bioseal with the FDA for Gauze Packing, X-ray Detectable.
Device ID | K882707 |
510k Number | K882707 |
Device Name: | GAUZE PACKING, X-RAY DETECTABLE |
Classification | Gauze/sponge, Internal, X-ray Detectable |
Applicant | BIOSEAL 350 NORTH PALM Brea, CA 92621 |
Contact | William L Runion |
Correspondent | William L Runion BIOSEAL 350 NORTH PALM Brea, CA 92621 |
Product Code | GDY |
CFR Regulation Number | 878.4450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-06-27 |
Decision Date | 1988-08-03 |