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

FLEXIBLE ARTHROSCOPE

K Number: K904465 · Decision Dec 20, 1990
Classifications
1
FEI Numbers
386
Registration Numbers
386
Same Product Code
680
Applicant Total
14
Review Days
80

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Basic Information

Device Name
FLEXIBLE ARTHROSCOPE
K Number
K904465
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Intramed Laboratories, Inc.
Date Received
October 1, 1990
Decision Date
December 20, 1990
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 Intramed Laboratories, Inc.

K Number Device Name
K953258 TITANIUM HEMOSTATIC CLIP
K942457 GRAFT THROMBECTOMY INSTRUMENTS
K931792 ARTHROSCOPE
K925283 VALVULOTOME
K934696 ANGIOSCOPE
K922114 ENDOSCOPIC RETRIEVAL BASKET
K914385 OPTICAL VALVULOTOME
K903528 LAPAROSCOPE
K902444 CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
K901010 FLEXIBLE CHOLEDOCHOSCOPE
Search all 14 clearances from Intramed Laboratories, Inc. →