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

STOCKERT-SHILEY CAPS HLM INTERFACE

K Number: K863541 · Decision Nov 18, 1986
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
51
Applicant Total
174
Review Days
68

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Basic Information

Device Name
STOCKERT-SHILEY CAPS HLM INTERFACE
K Number
K863541
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Shiley, Inc.
Date Received
September 11, 1986
Decision Date
November 18, 1986
Product Code
DTQ
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
DTQ Console, Heart-Lung Machine, Cardiopulmonary Bypass

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