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

PACEART WRIST ELECTRODES

K Number: K960721 · Decision Jul 18, 1996
Classifications
1
FEI Numbers
191
Registration Numbers
191
Same Product Code
328
Applicant Total
9
Review Days
147

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Basic Information

Device Name
PACEART WRIST ELECTRODES
K Number
K960721
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2360
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Paceart, Inc.
Date Received
February 22, 1996
Decision Date
July 18, 1996
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 Paceart, Inc.

K Number Device Name
K012407 PACEART TX3 CARDIAC EVENT RECORDER
K982090 PACEART HOME TRAK PLUS EASI EVENT RECORDER SYSTEM
K973141 HEART ACCESS PLUS CARDIAC EVENT RECORDER
K952065 PACEART CARDIOVOICE
K931296 PACEART CARDIOPHONE
K915632 PACEART CPTS-86/12
K880283 PACEART PACEMAKER PATIENT TEST SYST/TEL OPT CPTS
K870909 PACEMAKER FUNCTION ANALYZER