The following data is part of a premarket notification filed by Surgical Specialties, Inc. with the FDA for S1 Cavity Packing.
Device ID | K861445 |
510k Number | K861445 |
Device Name: | S1 CAVITY PACKING |
Classification | Gauze/sponge, Internal |
Applicant | SURGICAL SPECIALTIES, INC. P.O. BOX 310 Reading, PA 19607 |
Contact | George Erl |
Correspondent | George Erl SURGICAL SPECIALTIES, INC. P.O. BOX 310 Reading, PA 19607 |
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 | 1986-04-17 |
Decision Date | 1986-05-06 |