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

FINGER BONIOMETER BK7506

K Number: K831550 · Decision Jun 24, 1983
Classifications
1
FEI Numbers
89
Registration Numbers
89
Same Product Code
12
Applicant Total
278
Review Days
43

Basic Information

Device Name
FINGER BONIOMETER BK7506
K Number
K831550
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.1520
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
FRED SAMMONS, INC.
Date Received
May 12, 1983
Decision Date
June 24, 1983
Product Code
KQW
Advisory Committee
Orthopedic
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
KQW Goniometer, Nonpowered

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