FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇱 Israel

EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0

K Number: K100376 · Decision Aug 6, 2010
Classifications
1
FEI Numbers
72
Registration Numbers
72
Same Product Code
116
Applicant Total
12
Review Days
175

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Basic Information

Device Name
EVERON CENTRAL DISPLAY STATION - CDS, MODEL VERSION 1.0.0
K Number
K100376
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2300
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Earlysense, Ltd.
Date Received
February 12, 2010
Decision Date
August 6, 2010
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

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

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Other Clearances by Earlysense, Ltd.

K Number Device Name
K171836 EarlySense Bed Sensing Unit
K152911 EarlySense Insight Sytem
K151006 EarlySense Central Display Station (CDS)
K133661 CHAIR SENSING UNIT FOR EARLYSENSE SYSTEM
K131379 EARLYSENSE
K121885 EARLYSENSE CENTRAL DISPLAY SYSTEM
K120465 EARLYSENSE (EVERON) SYSTEM
K110521 EVERON CENTRAL DISPLAY STATION (CDS)
K092062 EVERON 1.0
K082465 EVERON
Search all 12 clearances from Earlysense, Ltd. →