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

K-FREE

K Number: K912587 · Decision Jul 30, 1991
Classifications
1
FEI Numbers
37
Registration Numbers
37
Same Product Code
165
Applicant Total
26
Review Days
48

Basic Information

Device Name
K-FREE
K Number
K912587
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
KATECHO, INC.
Date Received
June 12, 1991
Decision Date
July 30, 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)

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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
K003228 K-DEFIB/PACE MULTIFUCTION PEDIATRIC ELECTRODE, MODEL KDP-70A
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
Search all 26 clearances from KATECHO, INC. →