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

ARTHROSCOPE & ACCESSORIES

K Number: K921985 · Decision Jun 29, 1993
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
15
Review Days
427

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Basic Information

Device Name
ARTHROSCOPE & ACCESSORIES
K Number
K921985
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Optimed Technologies, Inc.
Date Received
April 28, 1992
Decision Date
June 29, 1993
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 Optimed Technologies, Inc.

K Number Device Name
K972520 OPTIVIEW
K955275 BOOSTER TROPHY 5 MOTORIZED SCOOTER
K955276 BOOSTER LITE 4 MOTORIZED SCOOTER
K955274 BOOSTER LITE 3 MOTORIZED SCOOTER
K943598 FLEXIBLE FIBER OPTIC LAPAROSCOPES
K926597 LAPAROSCOPE, GYNECOLOGIC (AND ACCESSORIES)
K921942 HYSTEROSCOPE (AND ACCESSORIES)
K922711 FLEXIBLE FIBER OPTIC GYNECOLOGIC ENDOSCOPE
K922826 FLEXIBLE FIBER OPTIC ENDOSCOPE
K921883 ENDOSCOPE
Search all 15 clearances from Optimed Technologies, Inc. →