Pedicraft, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pedicraft, Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pedicraft, Inc. has 5 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 5 cleared submissions from 1982 to 1993. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Pedicraft, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pedicraft, Inc.
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