FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

BJORK-SHILEY AORTIC GRAFT VALVE PROSTH

K Number: K791225 · Decision Aug 10, 1979
Classifications
1
FEI Numbers
27
Registration Numbers
27
Same Product Code
460
Applicant Total
174
Review Days
38

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Basic Information

Device Name
BJORK-SHILEY AORTIC GRAFT VALVE PROSTH
K Number
K791225
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3610
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
July 3, 1979
Decision Date
August 10, 1979
Product Code
DXY
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
DXY Implantable Pacemaker Pulse-Generator

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K901250 PLEXUS 2(TM) INFANT HOLLOW FIBER OXYGENATOR
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