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

EKG VEST

K Number: K932903 · Decision Feb 24, 1995
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
27
Review Days
618

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Basic Information

Device Name
EKG VEST
K Number
K932903
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Cardiotronics, Inc.
Date Received
June 16, 1993
Decision Date
February 24, 1995
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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Other Clearances by Cardiotronics, Inc.

K Number Device Name
K922064 MODEL #510 STEALTH-PLATE DISPERSIVE ELECTRODE
K923297 MODEL #340 STEALTH-TRODE+LS
K922173 MODEL # 830 ST ADULT STIMULATION PADS (STERILE)
K922227 MODEL #225-ST SHOCK-TRODE ADULT DEFIB PADS STERILE
K922172 MODEL # 230 ST STEALTH-TRODE DEFIB PADS (STERILE)
K921606 MODEL #125 CHILD STIMULATION PADS
K920086 SHOCK-PATCH ADULT DEFIBRILLATION PADS
K914725 COORDINATOR, CABLE INPUT
K911456 MODEL #110 STEALTH-TRODE CHILD DEFIB PADS
K912621 MODEL #911 STEALTH MULTI PADS
Search all 27 clearances from Cardiotronics, Inc. →