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

IMPLANTABLE ELECTRODE LEAD, MODEL 030-446

K Number: K874664 · Decision May 31, 1988
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
107
Review Days
200

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Basic Information

Device Name
IMPLANTABLE ELECTRODE LEAD, MODEL 030-446
K Number
K874664
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Telectronics, Inc.
Date Received
November 13, 1987
Decision Date
May 31, 1988
Product Code
DTB
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
DTB Permanent Pacemaker Electrode

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Other Clearances by Telectronics, Inc.

K Number Device Name
K890895 IMPLANTABLE ADAPTOR 033-380
K891231 OPTIMA MPT AND SPT PACEMAKERS
K890350 VS-1 SILICONE IMPLANT LEADS (NEW SERIAL # TUBE)
K884411 OPTIMA MPT AND SPT PACEMAKERS
K884278 IMPLANTABLE ELECTRODE LEADS 033-400,402 AND 436
K881837 OPTIMA MPT SERIES III PACEMAKER, 5281D AND 5282D
K864712 MODEL 1740 PERSONAL POCKET PROGRAMMER
K872766 IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
K865098 SLIMLINE UNIPOLAR ENDOCARDIAL PACING LEAD, 030-438
K871992 IMPLANTABLE PROGRAMMABLE CARDIAC PULSE GENERATORS
Search all 107 clearances from Telectronics, Inc. →