FDA 510(k), K173730, Kinsa QuickCare Thermometer
FDA 510(k), K173730, Kinsa QuickCare Thermometer
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510(K) Number: K173730
Device Name: Kinsa QuickCare Thermometer
Manufacturer: KINSA, Inc.
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 12/06/2017
Decision Date: 01/17/2018
Regulation Medical Specialty: General Hospital
Device Name: Kinsa QuickCare Thermometer
Manufacturer: KINSA, Inc.
Device Classification Name: Thermometer, Electronic, Clinical
Regulation Number: 880.2910
Classification Product Code: FLL
Date Received: 12/06/2017
Decision Date: 01/17/2018
Regulation Medical Specialty: General Hospital
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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