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

TRIAD-EP, PUSHBUTTON, CABLE INPUT TYPE

K Number: K883178 · Decision Nov 9, 1988
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
83
Applicant Total
27
Review Days
105

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Basic Information

Device Name
TRIAD-EP, PUSHBUTTON, CABLE INPUT TYPE
K Number
K883178
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5550
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cardiotronics, Inc.
Date Received
July 27, 1988
Decision Date
November 9, 1988
Product Code
DRO
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
DRO Pacemaker, Cardiac, External Transcutaneous (Non-Invasive)

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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
K914725 COORDINATOR, CABLE INPUT
K911456 MODEL #110 STEALTH-TRODE CHILD DEFIB PADS
Search all 27 clearances from Cardiotronics, Inc. →