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

IPOCON 7

K Number: K800749 · Decision Jul 28, 1980
Classifications
1
FEI Numbers
239
Registration Numbers
239
Same Product Code
36
Applicant Total
8
Review Days
115

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Basic Information

Device Name
IPOCON 7
K Number
K800749
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3025
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Ipos Luneburg
Date Received
April 4, 1980
Decision Date
July 28, 1980
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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K802976 CARBONACRYL
K800716 ORTHOTIC LEG GAIT CORRECTOR DEVICE
K800715 OHC DYNAMIC CLUB FOOT BRACE