Medcraft Corp.
FDA Regulatory Profile
Medcraft Corp. appears in FDA public data with 0 recalls, 5 510(k) clearances, 1 FDA inspection, and 0 compliance actions on record. Its most recent 510(k) clearance was granted on November 10, 1986.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 1
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K860467 | ELECTROSHOCK UNIT NEUROLOGY MODEL B-25 | November 10, 1986 |
| K791795 | COMP-ACT IV | September 27, 1979 |
| K760508 | ACCUTAPE 24 | August 30, 1976 |
| K760509 | TREADMILL, DIAGNOSTIC | August 30, 1976 |
| K760510 | MONITORING SYSTEM, REHABILITATION | August 30, 1976 |