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FDA 510(k), K173300, ViaTherm BOOST
FDA 510(k), K173300, ViaTherm BOOST
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510(K) Number: K173300
Device Name: ViaTherm BOOST
Manufacturer: ViaTherm Therapeutics, Llc.
Device Classification Name: diathermy, shortwave, for use in applying therapeutic deep heat
Regulation Number: 890.5290
Classification Product Code: IMJ
Date Received: 10/17/2017
Decision Date: 05/01/2018
Regulation Medical Specialty: Physical Medicine
Device Name: ViaTherm BOOST
Manufacturer: ViaTherm Therapeutics, Llc.
Device Classification Name: diathermy, shortwave, for use in applying therapeutic deep heat
Regulation Number: 890.5290
Classification Product Code: IMJ
Date Received: 10/17/2017
Decision Date: 05/01/2018
Regulation Medical Specialty: Physical Medicine
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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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