The following data is part of a premarket notification filed by Lorrex Health Products with the FDA for Triangular Sponges.
Device ID | K945606 |
510k Number | K945606 |
Device Name: | TRIANGULAR SPONGES |
Classification | Gauze/sponge, Internal, X-ray Detectable |
Applicant | LORREX HEALTH PRODUCTS 301 PENHORN AVE. Secaucus, NJ 07094 |
Contact | David M Pieratos |
Correspondent | David M Pieratos LORREX HEALTH PRODUCTS 301 PENHORN AVE. Secaucus, NJ 07094 |
Product Code | GDY |
CFR Regulation Number | 878.4450 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1994-11-15 |
Decision Date | 1994-12-28 |