FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DANEKSCOPE OPTI-PROBE

K Number: K943676 · Decision Nov 21, 1994
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
56
Review Days
118

Basic Information

Device Name
DANEKSCOPE OPTI-PROBE
K Number
K943676
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
DANEK MEDICAL, INC.
Date Received
July 26, 1994
Decision Date
November 21, 1994
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

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