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

Caretaker Remote Display App and Caretaker Software Library

K Number: K181196 · Decision Oct 3, 2018
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
190
Applicant Total
4
Review Days
149

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Basic Information

Device Name
Caretaker Remote Display App and Caretaker Software Library
K Number
K181196
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2910
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Caretaker Medical, LLC
Date Received
May 7, 2018
Decision Date
October 3, 2018
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 Caretaker Medical, LLC

K Number Device Name
K213699 CareTaker Monitor App
K163255 CareTaker Continuous Non-lnvasive Blood Pressure Monitor, CareTaker Wireless Vital Signs Monitor, CareTaker Physiological Monitor
K151499 CareTaker Continuous Non-Invasive Blood Pressure Monitor, CareTaker Wireless VItal Signs Monitor