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

CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP

K Number: K902444 · Decision Aug 30, 1990
Classifications
1
FEI Numbers
3
Registration Numbers
3
Same Product Code
8
Applicant Total
14
Review Days
90

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Basic Information

Device Name
CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
K Number
K902444
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1800
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Intramed Laboratories, Inc.
Date Received
June 1, 1990
Decision Date
August 30, 1990
Product Code
DQI
Advisory Committee
Cardiovascular
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
DQI Withdrawal/Infusion Pump

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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
K904465 FLEXIBLE ARTHROSCOPE
K903528 LAPAROSCOPE
K901010 FLEXIBLE CHOLEDOCHOSCOPE
Search all 14 clearances from Intramed Laboratories, Inc. →