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

CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.

K Number: K897026 · Decision Feb 26, 1990
Classifications
1
FEI Numbers
104
Registration Numbers
104
Same Product Code
400
Applicant Total
3
Review Days
69

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Basic Information

Device Name
CANYON MEDICAL FEMORAL BYPASS CANNULAE AND INTRO.
K Number
K897026
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4210
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Canyon Medical Products
Date Received
December 19, 1989
Decision Date
February 26, 1990
Product Code
DWF
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
DWF Catheter, Cannula And Tubing, Vascular, Cardiopulmonary Bypass

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DWF), ordered by most recent decision date.

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Other Clearances by Canyon Medical Products

K Number Device Name
K954181 CANYONS BI-DIRECTIONAL CHECK VALVE
K874899 CANYON MEDICAL FEMORAL BYPASS CANNULAE