The following data is part of a premarket notification filed by Amsco Sterile Recoveries, Inc. with the FDA for Non-linting Delivery Blanket.
| Device ID | K932035 |
| 510k Number | K932035 |
| Device Name: | NON-LINTING DELIVERY BLANKET |
| Classification | Table, Obstetric (and Accessories) |
| 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 | KNC |
| CFR Regulation Number | 884.4900 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-04-27 |
| Decision Date | 1994-05-26 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00812564039651 | K932035 | 000 |
| 00810019800016 | K932035 | 000 |
| 00812564037244 | K932035 | 000 |
| 00812564037282 | K932035 | 000 |
| 00812564037312 | K932035 | 000 |
| 00812564037442 | K932035 | 000 |
| 00812564035592 | K932035 | 000 |
| 00812564036513 | K932035 | 000 |
| 00812564039378 | K932035 | 000 |
| 00810019800405 | K932035 | 000 |