FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

CARDIOVASCULAR INSTRUMENTS-VARIOUS

K Number: K791710 · Decision Sep 12, 1979
Classifications
1
FEI Numbers
313
Registration Numbers
313
Same Product Code
70
Applicant Total
140
Review Days
16

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Basic Information

Device Name
CARDIOVASCULAR INSTRUMENTS-VARIOUS
K Number
K791710
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
870.4500
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Edward Weck, Inc.
Date Received
August 27, 1979
Decision Date
September 12, 1979
Product Code
DWS
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
DWS Instruments, Surgical, Cardiovascular

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