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

MODEL C UNIPOLAR ENDOCARDIAL LEAD

K Number: K811877 · Decision Aug 3, 1981
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
34
Review Days
33

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Basic Information

Device Name
MODEL C UNIPOLAR ENDOCARDIAL LEAD
K Number
K811877
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cook Pacemaker Corp.
Date Received
July 1, 1981
Decision Date
August 3, 1981
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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K915188 MODEL P IN-LINE BIPOLAR ENDOCARDIAL TINED LEAD
K905403 MODEL 340 SERIES UNIPOLAR & MODEL 5000B PROGRAMMER
K863582 MODEL 725TH HANDHELD TRANSCEIVER (PROGRAMMER)
K861559 SERIES (T) PROGRAMMABLE CARDIAC PULSE GENERATORS
K860202 MODEL 327D, SERIES R UNIPOLAR CARDIAC PULSE GENER.
K860466 MODEL 329D, SERIERS R BIOPOLAR CARDIAC PUL. GEN.
K854919 BIPOLAR CARDIAC PULSE GENERATOR WITH TELEMETRY
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