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FDA 510(k), K882816, PULSAR EM
FDA 510(k), K882816, PULSAR EM
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510(K) Number: K882816
Device Name: PULSAR EM
Manufacturer: LARRY INMAN
Device Classification Name: Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
Regulation Number: ILX
Classification Product Code: 07/08/1988
Date Received: 04/27/1989
Decision Date: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: PULSAR EM
Manufacturer: LARRY INMAN
Device Classification Name: Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
Regulation Number: ILX
Classification Product Code: 07/08/1988
Date Received: 04/27/1989
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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