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

GRAFT THROMBECTOMY INSTRUMENTS

K Number: K942457 · Decision Feb 7, 1995
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
14
Review Days
259

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Basic Information

Device Name
GRAFT THROMBECTOMY INSTRUMENTS
K Number
K942457
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intramed Laboratories, Inc.
Date Received
May 24, 1994
Decision Date
February 7, 1995
Product Code
MCW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
MCW Catheter, Peripheral, Atherectomy

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Other Clearances by Intramed Laboratories, Inc.

K Number Device Name
K953258 TITANIUM HEMOSTATIC CLIP
K931792 ARTHROSCOPE
K925283 VALVULOTOME
K934696 ANGIOSCOPE
K922114 ENDOSCOPIC RETRIEVAL BASKET
K914385 OPTICAL VALVULOTOME
K904465 FLEXIBLE ARTHROSCOPE
K903528 LAPAROSCOPE
K902444 CLEARVIEW(TM) ANGIOSCOPIC IRRIGATION PUMP
K901010 FLEXIBLE CHOLEDOCHOSCOPE
Search all 14 clearances from Intramed Laboratories, Inc. →