The following data is part of a premarket notification filed by Mr Associates, Inc. with the FDA for M.r. Assoc. Basket Retrievers.
| Device ID | K800970 |
| 510k Number | K800970 |
| Device Name: | M.R. ASSOC. BASKET RETRIEVERS |
| Classification | Endoscopic Grasping/cutting Instrument, Non-powered |
| Applicant | MR ASSOCIATES, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | OCZ |
| CFR Regulation Number | 876.1500 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1980-04-23 |
| Decision Date | 1980-05-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10816207020508 | K800970 | 000 |
| 10816207020119 | K800970 | 000 |
| 10816207020096 | K800970 | 000 |
| 10816207020089 | K800970 | 000 |
| 10816207020072 | K800970 | 000 |
| 10816207020065 | K800970 | 000 |
| 10816207020058 | K800970 | 000 |
| 10816207020041 | K800970 | 000 |
| 10816207020034 | K800970 | 000 |
| 10816207020027 | K800970 | 000 |
| 10816207020010 | K800970 | 000 |
| 10816207020126 | K800970 | 000 |
| 10816207020393 | K800970 | 000 |
| 00816207020495 | K800970 | 000 |
| 10816207020485 | K800970 | 000 |
| 10816207020478 | K800970 | 000 |
| 10816207020461 | K800970 | 000 |
| 10816207020454 | K800970 | 000 |
| 10816207020447 | K800970 | 000 |
| 10816207020430 | K800970 | 000 |
| 10816207020423 | K800970 | 000 |
| 10816207020416 | K800970 | 000 |
| 10816207020409 | K800970 | 000 |
| 10816207020003 | K800970 | 000 |