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FDA 510(k), K030226, THOR DDII 830CL3 LASER SYSTEM
FDA 510(k), K030226, THOR DDII 830CL3 LASER SYSTEM
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$149.00 USD
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510(K) Number: K030226
Device Name: THOR DDII 830CL3 LASER SYSTEM
Manufacturer: M. JOYCE HEINRICH
Device Classification Name: Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Regulation Number: NHN
Classification Product Code: 01/22/2003
Date Received: 02/10/2003
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: THOR DDII 830CL3 LASER SYSTEM
Manufacturer: M. JOYCE HEINRICH
Device Classification Name: Powered Light Based Laser Non-Thermal Instrument With Non-Heating Effect For Adjunctive Use In Pain Therapy
Regulation Number: NHN
Classification Product Code: 01/22/2003
Date Received: 02/10/2003
Decision Date: Substantially Equivalent (SESE)
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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