Pedicraft, Inc.
FDA Regulatory Profile
Pedicraft, 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 April 20, 1993.
Summary
- Total Recalls
- 0
- 510(k) Clearances
- 5
- Inspections
- 5
- Compliance Actions
- 0
Recent 510(k) Clearances
| K-Number | Device | Date |
|---|
| K925949 | PEDICRAGT BASSINET | April 20, 1993 |
| K925817 | HEAD & FOOT END DROP PEDI-CRIB | April 20, 1993 |
| K905629 | PEDICRAFT INFANT REFLUX WEDGE | March 13, 1991 |
| K905630 | INFANT REFLUX SLING | March 13, 1991 |
| K821773 | PEDICRAFT BED, MODEL B2944 | June 23, 1982 |