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

SLIM VENT BIPO PACING LEAD USING A90 INSUL,#30-284

K Number: K852916 · Decision Jul 29, 1985
Classifications
1
FEI Numbers
273
Registration Numbers
273
Same Product Code
701
Applicant Total
107
Review Days
35

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Basic Information

Device Name
SLIM VENT BIPO PACING LEAD USING A90 INSUL,#30-284
K Number
K852916
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Telectronics, Inc.
Date Received
June 24, 1985
Decision Date
July 29, 1985
Product Code
DYB
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
DYB Introducer, Catheter

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Other Clearances by Telectronics, Inc.

K Number Device Name
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K884411 OPTIMA MPT AND SPT PACEMAKERS
K884278 IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436
K881837 OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D
K874664 IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
K864712 MODEL 1740 PERSONAL POCKET PROGRAMMER
K872766 IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
K865098 SLIMLINE UNIPOLAR ENDOCARDIAL PACING LEAD, 030-438
Search all 107 clearances from Telectronics, Inc. →