Medron, Inc.
FDA Regulatory Profile
Medron, Inc. appears in FDA public data with 0 recalls, 3 510(k) clearances, 5 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on May 6, 2020.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 3
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K192283 | MEDRON Vessel Dilator - 6F x 22cm HDPE Dilator, MEDRON Vessel Dilator - 15.5F - 17.5F HDPE Dilator | May 6, 2020 |
| K971897 | CONTINUOUS ARTERIOVENOUS HEMOFILTRATION CATHETER 10 FR (CAVH) | October 21, 1997 |
| K940775 | INJECTION CAP | June 15, 1994 |