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

COORDINATOR, CABLE INPUT

K Number: K914725 · Decision Nov 5, 1991
Classifications
1
FEI Numbers
177
Registration Numbers
177
Same Product Code
574
Applicant Total
27
Review Days
15

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Basic Information

Device Name
COORDINATOR, CABLE INPUT
K Number
K914725
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2340
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Cardiotronics, Inc.
Date Received
October 21, 1991
Decision Date
November 5, 1991
Product Code
DPS
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
DPS Electrocardiograph

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Other Clearances by Cardiotronics, Inc.

K Number Device Name
K932903 EKG VEST
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
K911456 MODEL #110 STEALTH-TRODE CHILD DEFIB PADS
K912621 MODEL #911 STEALTH MULTI PADS
Search all 27 clearances from Cardiotronics, Inc. →