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

ARTHROSCOPE

K Number: K942029 · Decision Nov 8, 1995
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
28
Review Days
561

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Basic Information

Device Name
ARTHROSCOPE
K Number
K942029
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Surgical Technologies, Inc.
Date Received
April 26, 1994
Decision Date
November 8, 1995
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 Surgical Technologies, Inc.

K Number Device Name
K941992 CYSTOSCOPE
K946136 INFINITECH LIGHTED INFUSION CANNULA
K952566 OSCILFLATOR
K951918 SURGICAL TECHNOLOGIES, INC. SYRINGE
K950683 ARTHROGRAM TRAY
K946135 INFINITECH ASPIRATING LASER PROBE
K946181 INFINITECH SOFT TIP FLUTE NEEDLE
K942030 BIOPSY SCISSORS
K942482 PRESSURE MONITORING EXTENSION
K941161 FLEXIBLE GRASPING FORCEPS
Search all 28 clearances from Surgical Technologies, Inc. →