The following data is part of a premarket notification filed by Amsco Sterile Recoveries, Inc. with the FDA for Amsco Sterile Recoveries Surgical Packs.
| Device ID | K932522 |
| 510k Number | K932522 |
| Device Name: | AMSCO STERILE RECOVERIES SURGICAL PACKS |
| Classification | Applicator, Ent Drug |
| Applicant | AMSCO STERILE RECOVERIES, INC. 28100 U.S. HWY, 19N., STE. 201 Clearwater, FL 34621 |
| Contact | Denise A Schottler |
| Correspondent | Denise A Schottler AMSCO STERILE RECOVERIES, INC. 28100 U.S. HWY, 19N., STE. 201 Clearwater, FL 34621 |
| Product Code | LRD |
| CFR Regulation Number | 874.5220 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-25 |
| Decision Date | 1994-09-09 |