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

STAYHEALTHY HEALTH KIOSK, STAYHEALTHY HEALTHCENTER KIOSK

K Number: K123539 · Decision Apr 22, 2013
Classifications
1
FEI Numbers
428
Registration Numbers
428
Same Product Code
1216
Applicant Total
3
Review Days
157

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Basic Information

Device Name
STAYHEALTHY HEALTH KIOSK, STAYHEALTHY HEALTHCENTER KIOSK
K Number
K123539
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.1130
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Stayhealthy, Inc.
Date Received
November 16, 2012
Decision Date
April 22, 2013
Product Code
DXN
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
Y

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DXN System, Measurement, Blood-Pressure, Non-Invasive

Similar 510(k) Clearances

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

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Other Clearances by Stayhealthy, Inc.

K Number Device Name
K101807 STAYHEALTHY BODY COMPOSITION MONITOR-BCM
K052522 STAYHEALTHY BODY COMPOSITION ANALYZER, MODELS BC1 AND BC2