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

PROCAST

K Number: K791831 · Decision Sep 24, 1979
Classifications
1
FEI Numbers
239
Registration Numbers
239
Same Product Code
36
Applicant Total
40
Review Days
6

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Basic Information

Device Name
PROCAST
K Number
K791831
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Medical Specialties, Inc.
Date Received
September 18, 1979
Decision Date
September 24, 1979
Product Code
ITG
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
ITG Bandage, Cast

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