The following data is part of a premarket notification filed by Smith & Nephew United, Inc. with the FDA for Profore Four-layer Bandage System Kit.
| Device ID | K961775 |
| 510k Number | K961775 |
| Device Name: | PROFORE FOUR-LAYER BANDAGE SYSTEM KIT |
| Classification | Gauze/sponge, Internal |
| Applicant | SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
| Contact | Jim Irvin |
| Correspondent | Jim Irvin SMITH & NEPHEW UNITED, INC. 11775 STARKLEY RD. P.O.BOX 1970 Largo, FL 34649 -1970 |
| 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 | 1996-05-08 |
| Decision Date | 1996-07-16 |