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

RV PACING LEAD

K Number: K962467 · Decision Sep 17, 1996
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
128
Applicant Total
883
Review Days
84

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Basic Information

Device Name
RV PACING LEAD
K Number
K962467
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.3680
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Abbott Laboratories
Date Received
June 25, 1996
Decision Date
September 17, 1996
Product Code
LDF
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
LDF Electrode, Pacemaker, Temporary

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