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

STOCKERT COMPACT SYSTEM

K Number: K982014 · Decision Sep 4, 1998
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
51
Applicant Total
13
Review Days
88

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Basic Information

Device Name
STOCKERT COMPACT SYSTEM
K Number
K982014
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.4220
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stoeckert Instrumente
Date Received
June 8, 1998
Decision Date
September 4, 1998
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

Similar 510(k) Clearances

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

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Other Clearances by Stoeckert Instrumente

K Number Device Name
K002273 STOCKERT A272 SERIES PEDIATRIC AORTIC CANNULAE
K001961 STOCKERT A242 AND A252 SERIES ARTERIAL FEMORAL CANNULAE
K002118 STOCKERT COMPACT SYSTEM VERSION 2.0
K992635 INTERFACE MODULE IDDD
K990512 STOCKERT POWER SUPPLY UNIT FOR S3 COMPONENTS
K972321 S3 MAST PUMP
K971520 S3 CYCLIC RPM CONTROL
K962320 S3 CARDIOPLEGIA CONTROL
K955152 STOCKERT S3 UPS, LVL CTRL BUBB. DET., DUAL PRESS. CTRL., TEMP MONT., TIMER
K955038 STOCKERT S3 DOUBLE HEAD PUMP MODULE
Search all 13 clearances from Stoeckert Instrumente →