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

OBTHOSES

K Number: K821641 · Decision Jun 11, 1982
Classifications
1
FEI Numbers
519
Registration Numbers
519
Same Product Code
51
Applicant Total
278
Review Days
8

Basic Information

Device Name
OBTHOSES
K Number
K821641
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
FRED SAMMONS, INC.
Date Received
June 3, 1982
Decision Date
June 11, 1982
Product Code
IQI
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
IQI Orthosis, Limb Brace

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