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

CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE

K Number: K891905 · Decision Jun 5, 1989
Classifications
1
FEI Numbers
24
Registration Numbers
24
Same Product Code
486
Applicant Total
96
Review Days
70

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Basic Information

Device Name
CARDIOVASCULAR PERMANENT PACEMAKER ELECTRODE
K Number
K891905
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Pacesetter Systems
Date Received
March 27, 1989
Decision Date
June 5, 1989
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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K885267 VS-1 MODEL NUMBER 251K PULSE GENERATOR
K890547 SIEMENS ELEMA MODELS 4025 AND 4026 ADAPTERS
K884733 AFP MODEL 262T PULSE GENERATOR
K883087 PROLOG MP 658M PULSE GENERATOR
K874205 ENDOCARDIAL SCREW-IN LEAD, MODEL 1018T
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