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

VITATRACE

K Number: K893425 · Decision Jul 14, 1989
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
27
Review Days
73

Basic Information

Device Name
VITATRACE
K Number
K893425
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
LECTEC CORP.
Date Received
May 2, 1989
Decision Date
July 14, 1989
Product Code
DRX
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
DRX Electrode, Electrocardiograph

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