MICROSNARE
Catheter, Percutaneous
MICROVENA CORP.
The following data is part of a premarket notification filed by Microvena Corp. with the FDA for Microsnare.
Pre-market Notification Details
| Device ID | K925439 |
| 510k Number | K925439 |
| Device Name: | MICROSNARE |
| Classification | Catheter, Percutaneous |
| Applicant | MICROVENA CORP. 3600 LABORE RD. #1 Vadnais Heights, MN 55110 |
| Contact | Michael Renner |
| Correspondent | Michael Renner MICROVENA CORP. 3600 LABORE RD. #1 Vadnais Heights, MN 55110 |
| Product Code | DQY |
| CFR Regulation Number | 870.1250 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1992-10-28 |
| Decision Date | 1993-09-24 |
Trademark Results [MICROSNARE]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 MICROSNARE 88439342 not registered Live/Pending |
Forensic IT, Inc. 2019-05-21 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.