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

ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE

K Number: K042302 · Decision Oct 26, 2004
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
165
Applicant Total
33
Review Days
62

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Basic Information

Device Name
ZOLL AUTOCLAVABLE INTERNAL HANDLES, ZOLL AUTOCLAVABLE INTERNAL HANDLES WITH INTEGRATED ELECTRODES, ZOLL AUTOCLAVABLE
K Number
K042302
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
870.5300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Zoll Medical Corp
Date Received
August 25, 2004
Decision Date
October 26, 2004
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 Zoll Medical Corp

K Number Device Name
K133484 ZOLL X SERIES
K112660 POCKETCPR
K090989 ZOLL R SERIES WITH NIBP AND ETCO2 OPTIONS, ZOLL R SERIES
K042007 ZOLL E SERIES DEFIBRILLATOR
K042417 ZOLL M SERIES ETC02 LOFLO OPTION
K033474 ZOLL AED PLUS
K032691 ZOLL AUTOCLAVABLE INTERNAL HANDLES
K032439 ZOLL M SERIES WITH RECTILINEAR BI-PHASIC OPTION (M SERIES BI-PHASIC)
K032363 ZOLL M SERIES NIBP OPTION
K011541 ZOLL PAD WITH CPR AID
Search all 33 clearances from Zoll Medical Corp →