Pedicraft, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
5
Inspections
5
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K925817HEAD & FOOT END DROP PEDI-CRIBApril 20, 1993
K925949PEDICRAGT BASSINETApril 20, 1993
K905629PEDICRAFT INFANT REFLUX WEDGEMarch 13, 1991
K905630INFANT REFLUX SLINGMarch 13, 1991
K821773PEDICRAFT BED, MODEL B2944June 23, 1982