The following data is part of a premarket notification filed by Neometrics, Inc with the FDA for Bard Snare Retrieval Kit.
| Device ID | K152560 |
| 510k Number | K152560 |
| Device Name: | Bard Snare Retrieval Kit |
| Classification | Device, Percutaneous Retrieval |
| Applicant | NEOMETRICS, INC 2605 FERNBROOK LANE, SUITE J Plymouth, MN 55447 |
| Contact | Dave Liebl |
| Correspondent | Dave Liebl NEOMETRICS, INC 2605 FERNBROOK LANE, SUITE J Plymouth, MN 55447 |
| Product Code | MMX |
| CFR Regulation Number | 870.5150 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2015-09-09 |
| Decision Date | 2015-10-23 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00857834006551 | K152560 | 000 |
| 00857834006544 | K152560 | 000 |