Interrad Medical, Inc.
Interrad Medical, Inc. appears in FDA public data with 0 recalls, 7 510(k) clearances, 2 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on April 12, 2021.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 7
- Inspections
- 2
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|---|---|
| K210629 | SecurAcath | April 12, 2021 |
| K180994 | SecurAcath 10F, SecurAcath 12F, SecurAcath 5F, SecurAcath 5F, SecurAcath 6F, SecurAcath 7F/SecurAcat | July 9, 2019 |
| K180769 | SecurAcath | June 26, 2018 |
| K120935 | SECURACATH | April 27, 2012 |
| K092306 | SECURACATH UNIVERSAL | July 9, 2010 |
| K083081 | MODIFICATION TO SECURACATH, MODEL: SPK01 | March 4, 2009 |
| K082047 | SECURACATH CATHETER, MODEL SPK01 | September 30, 2008 |