Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1868391137
Device Listing 1868391137
Listing Summary
#
Listing key
1868391137
Premarket submission
K905629
Device
PEDICRAFT INFANT REFLUX WEDGE
Applicant
Pedicraft, Inc.
Product code
FRP
Decision date
1991-03-13
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
605
1043568
1043568
PEDICRAFT, INC.
1
N
2026-01-01
4134 ST. AUGUSTINE RD. P.O. BOX 5969 JACKSONVILLE FL US 32247