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

TELEMEDICINE SYSTEM MODEL VMS-01

K Number: K062662 · Decision Nov 21, 2006
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
3
Review Days
75

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Basic Information

Device Name
TELEMEDICINE SYSTEM MODEL VMS-01
K Number
K062662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medic4all (Israel) , Ltd.
Date Received
September 7, 2006
Decision Date
November 21, 2006
Product Code
DRG
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
DRG Transmitters And Receivers, Physiological Signal, Radiofrequency

Similar 510(k) Clearances

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

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Other Clearances by Medic4all (Israel) , Ltd.

K Number Device Name
K062127 MEDIC4ALL TELEMEDICINE SYSTEM, MODEL VMS-01 (NIBP)
K061502 MEDIC4ALL TELEMEDICINE SYSTEM VMS-01