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FDA 510(k), K080102, TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
FDA 510(k), K080102, TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
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510(K) Number: K080102
Device Name: TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
Manufacturer: ESCADA INTERNATIONAL, INC.
Device Classification Name: lamp, infrared, therapeutic heating
Regulation Number: 890.5500
Classification Product Code: ILY
Date Received: 01/14/2008
Decision Date: 08/20/2008
Regulation Medical Specialty: Physical Medicine
Device Name: TQ SOLO AND SOLO PRO AND LS50 ACCESSORY AND MR4 MULTI RADIANCE THERAPY SYSTEM
Manufacturer: ESCADA INTERNATIONAL, INC.
Device Classification Name: lamp, infrared, therapeutic heating
Regulation Number: 890.5500
Classification Product Code: ILY
Date Received: 01/14/2008
Decision Date: 08/20/2008
Regulation Medical Specialty: Physical Medicine
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- 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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