Mercator Medsystems, Inc.
Mercator Medsystems, Inc. appears in FDA public data with 0 recalls, 5 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on August 2, 2021.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K210339 | Bullfrog Micro-Infusion Device | August 2, 2021 |
| K161402 | Bullfrog Micro-Infusion Device | August 18, 2016 |
| K153501 | Bullfrog Micro-Infusion Device | April 15, 2016 |
| K131401 | BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER | July 2, 2013 |
| K062752 | MERCATOR MICROSYRINGE II INFUSION CATHETER | December 7, 2006 |