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

HUMERAL FRACTURE CAST BRACE

K Number: K811343 · Decision May 28, 1981
Classifications
1
FEI Numbers
503
Registration Numbers
503
Same Product Code
51
Applicant Total
20
Review Days
16

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Basic Information

Device Name
HUMERAL FRACTURE CAST BRACE
K Number
K811343
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3475
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Applicant
Deseret Medical, Inc.
Date Received
May 12, 1981
Decision Date
May 28, 1981
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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