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

MODEL #110 STEALTH-TRODE CHILD DEFIB PADS

K Number: K911456 · Decision Oct 16, 1991
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
27
Review Days
196

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Basic Information

Device Name
MODEL #110 STEALTH-TRODE CHILD DEFIB PADS
K Number
K911456
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Cardiotronics, Inc.
Date Received
April 3, 1991
Decision Date
October 16, 1991
Product Code
LDD
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
LDD Dc-Defibrillator, Low-Energy, (Including Paddles)

Similar 510(k) Clearances

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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
K912621 MODEL #911 STEALTH MULTI PADS
Search all 27 clearances from Cardiotronics, Inc. →