FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A

K Number: K003228 · Decision Dec 14, 2000
Classifications
1
FEI Numbers
64
Registration Numbers
64
Same Product Code
227
Applicant Total
26
Review Days
59

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Basic Information

Device Name
K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
K Number
K003228
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
870.5310
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Katecho, Inc.
Date Received
October 16, 2000
Decision Date
December 14, 2000
Product Code
MKJ
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
MKJ Automated External Defibrillators (Non-Wearable)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MKJ), ordered by most recent decision date.

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Other Clearances by Katecho, Inc.

K Number Device Name
K012404 K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-85
K010543 KM-30 TENS ELECTRODE
K002806 K-DEFIB/PACE, MODEL KDP-60A
K000870 KM-10 TENS ELECTRODE
K993745 K-DEFIB/PACE ADULT ELECTRODE, MODEL KDP-80
K991007 K-DEFIB/PACE RADIOLUCENT ADULT ELECTRODE, MODEL KRT-60
K981737 K-DEFIB/PACE ADULT ELECTRODE MODEL NUMBER KDP-60
K954504 K-DEFIB/PACE PEDIATRIC ELECTRODE
K934692 K-DEFIB/PACE PEDIATRIC ELECTRODE
K940801 K-KLIP
Search all 26 clearances from Katecho, Inc. →