Pedicraft, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
FDA 510(k) Regulatory Record - Pedicraft, Inc. General Hospital ✕
5 devices
Cleared
Apr 20, 1993
HEAD & FOOT END DROP PEDI-CRIB
General Hospital
154d
Cleared
Apr 20, 1993
PEDICRAGT BASSINET
General Hospital
147d
Cleared
Mar 13, 1991
PEDICRAFT INFANT REFLUX WEDGE
General Hospital
89d
Cleared
Mar 13, 1991
INFANT REFLUX SLING
General Hospital
89d
Cleared
Jun 23, 1982
PEDICRAFT BED, MODEL B2944
General Hospital
7d