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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
K925949
PEDICRAGT BASSINET
April 20, 1993
K925817
HEAD & FOOT END DROP PEDI-CRIB
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