ClearanceBrief
Company ยท US

Pedicraft, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1982 to 1993. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
FMSBed, Pediatric Open Hospital3
FRPHolder, Infant Position2

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Apr 20, 1993K925949PEDICRAGT BASSINET
Pedicraft, Inc.
FMS
Apr 20, 1993K925817HEAD & FOOT END DROP PEDI-CRIB
Pedicraft, Inc.
FMS
Mar 13, 1991K905630INFANT REFLUX SLING
Pedicraft, Inc.
FRP
Mar 13, 1991K905629PEDICRAFT INFANT REFLUX WEDGE
Pedicraft, Inc.
FRP
Jun 23, 1982K821773PEDICRAFT BED, MODEL B2944
Pedicraft, Inc.
FMS

Latest recalls

DateFirm and productCodeLinked 510(k)
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