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

MODEL #810 STEALTH-STIM ADULT STIMULATION PADS

K Number: K913226 · Decision Sep 4, 1991
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
27
Review Days
47

Basic Information

Device Name
MODEL #810 STEALTH-STIM ADULT STIMULATION PADS
K Number
K913226
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
CARDIOTRONICS, INC.
Date Received
July 19, 1991
Decision Date
September 4, 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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