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

LECTEC NON-INVASIVE PACING ELECTRODE

K Number: K872012 · Decision Jun 29, 1987
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
83
Applicant Total
27
Review Days
34

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Basic Information

Device Name
LECTEC NON-INVASIVE PACING ELECTRODE
K Number
K872012
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5550
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Lectec Corp.
Date Received
May 26, 1987
Decision Date
June 29, 1987
Product Code
DRO
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
DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

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K893425 VITATRACE
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