Revivant Corp.
FDA Regulatory Profile
Revivant Corp. appears in FDA public data with 0 recalls, 4 510(k) clearances, 0 FDA inspections, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on March 11, 2004.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 4
- Inspections
- 0
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K040453 | AUTOPULSE RESUSCITATION SYSTEM, MODEL 100 | March 11, 2004 |
| K032852 | MODIFICATION TO: AUTOPULSE RESUSCITATION SYSTEM MODEL 100 | November 12, 2003 |
| K022345 | AUTOPULSE RESUSCITATION SYSTEM | August 15, 2002 |
| K011046 | AUTOPULSE, MODEL 100 | October 25, 2001 |