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Pedicraft, Inc.
FDA Regulatory Profile
Summary
Total Recalls
0
510(k) Clearances
5
Inspections
5
Compliance Actions
0
Recent 510(k) Clearances
K-Number
Device
Date
K925817
HEAD & FOOT END DROP PEDI-CRIB
April 20, 1993
K925949
PEDICRAGT BASSINET
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