Pedicraft, Inc.
FDA 510(k) & PMA Approved Devices — 5 products
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Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K925817 | HEAD & FOOT END DROP PEDI-CRIB | FMS | 1993-04-20 | View |
| 510(k) | K925949 | PEDICRAGT BASSINET | FMS | 1993-04-20 | View |
| 510(k) | K905630 | INFANT REFLUX SLING | FRP | 1991-03-13 | View |
| 510(k) | K905629 | PEDICRAFT INFANT REFLUX WEDGE | FRP | 1991-03-13 | View |
| 510(k) | K821773 | PEDICRAFT BED, MODEL B2944 | FMS | 1982-06-23 | View |
No matching devices.
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