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

MINISCOPE

K Number: K910587 · Decision May 13, 1991
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
12
Review Days
90

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Basic Information

Device Name
MINISCOPE
K Number
K910587
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Citation Medical Corp.
Date Received
February 12, 1991
Decision Date
May 13, 1991
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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Other Clearances by Citation Medical Corp.

K Number Device Name
K951941 CITATION MULTIPLE USE DELTA SCOPE
K945390 CITATION DELTA SCOPE
K946290 CITATION POWER TOOL
K951249 CITATION SINUSCOPE
K944976 BRONCHOSCOPE,NON-RIGID
K940847 ENDOSCOPIC PLANTAR FASCIA KIT
K941563 THE BIOPSY TOOL
K924494 CITSCOPE, BENDABLE -- MODIFICATION
K922144 CITSCOPE (MODEL EXTENSIONS)
K921692 INTEGRATED VIDEO SYSTEM
Search all 12 clearances from Citation Medical Corp. →