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

PROVEST-PROTECTIVE RESTRAINT

K Number: K971561 · Decision Jul 14, 1997
Classifications
1
FEI Numbers
109
Registration Numbers
109
Same Product Code
133
Applicant Total
1
Review Days
76

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Basic Information

Device Name
PROVEST-PROTECTIVE RESTRAINT
K Number
K971561
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.6760
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Jemm Medical Products
Date Received
April 29, 1997
Decision Date
July 14, 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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