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

VITALCONNECT PLATFORM BY VITAL CONNECT INC.

K Number: K132447 · Decision Apr 3, 2014
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
10
Review Days
240

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Basic Information

Device Name
VITALCONNECT PLATFORM BY VITAL CONNECT INC.
K Number
K132447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Vitalconnect, Inc.
Date Received
August 6, 2013
Decision Date
April 3, 2014
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 Vitalconnect, Inc.

K Number Device Name
K242129 VitalRhythm
K193343 Vista Solution Monitoring Kit, Vista Solution 2 10-day Evaluation Kit, VistaTablet 2 (Boxed)
K192757 VitalPatch 5D Biosensor - single, VitalPatch 7D Biosensor - single, VitalPatch 5D Biosensor – bag of 20, VitalPatch 7D Biosensor – bag of 20
K190916 VitalPatch 7D Biosensor - single, VitalPatch 7D Biosensor - bag of 20
K183078 VitalConnect Platform, VitalPatch Biosensor
K163453 VitalPatch® VitalConnect Platform
K170973 VitalWatch Software User Interface
K152139 Vital Connect Platform, HealthPatch MD, VitalPatch
K141167 VITALCONNECT PLATFORM (CONSISTING OF VITALCONNECT SENSOR, RELAY SOFTWARE LIBRARY AND SECURE SERVER SOFTWARE LIBRARY)