FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

PEDO CUSH PEDO CUDDLE

K Number: K972446 · Decision Nov 13, 1997
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
133
Applicant Total
1
Review Days
136

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Basic Information

Device Name
PEDO CUSH PEDO CUDDLE
K Number
K972446
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6760
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cavity Free Kids, Inc.
Date Received
June 30, 1997
Decision Date
November 13, 1997
Product Code
FMQ
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FMQ Restraint, Protective

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