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

ZOLL RESCUENETLINK

K Number: K111296 · Decision Oct 27, 2011
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
116
Applicant Total
21
Review Days
171

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Basic Information

Device Name
ZOLL RESCUENETLINK
K Number
K111296
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Zoll Medical Corporation, World Wide Headquarters
Date Received
May 9, 2011
Decision Date
October 27, 2011
Product Code
MSX
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
MSX System, Network And Communication, Physiological Monitors

Similar 510(k) Clearances

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Other Clearances by Zoll Medical Corporation, World Wide Headquarters

K Number Device Name
K133239 ZOLL E SERIES
K133269 ZOLL X SERIES
K120406 ZOLL FULLY AUTOMATIC AED PLUS
K120907 ZOLL R SERIES
K112761 ZOLL PROPAQ MD
K112432 ZOLL X SERIES
K111594 ZOLL E SERIES
K110361 ZOLL R SERIES WITH 2010 AHA GUIDELINES SOFTWARE UPDATE
K110154 ZOLL AED PLUS WITH 2010 AHA GUIDLINES SOFTWARE UPDATE
K110168 ZOLL E SERIES WITH 2010 AHA GUIDLINES SOFTWARE UPDATE
Search all 21 clearances from Zoll Medical Corporation, World Wide Headquarters →