FDA 510(k), K062042, PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)
FDA 510(k), K062042, PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)
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510(K) Number: K062042
Device Name: PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)
Manufacturer: PLETHORA SOLUTIONS
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 07/19/2006
Decision Date: 09/06/2006
Regulation Medical Specialty:
Device Name: PLETHORA SOLUTIONS SEXUAL ASSESSMENT MONITOR (SAM)
Manufacturer: PLETHORA SOLUTIONS
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 07/19/2006
Decision Date: 09/06/2006
Regulation Medical Specialty:
- 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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