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

TRACET AG 4000

K Number: K904512 · Decision Jan 31, 1991
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
27
Review Days
121

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Basic Information

Device Name
TRACET AG 4000
K Number
K904512
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Lectec Corp.
Date Received
October 2, 1990
Decision Date
January 31, 1991
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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