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FDA 510(k), K841202, DACOMED RIGISCAN SYSTEM
FDA 510(k), K841202, DACOMED RIGISCAN SYSTEM
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510(K) Number: K841202
Device Name: DACOMED RIGISCAN SYSTEM
Manufacturer: DACOMED CORP.
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 03/21/1984
Decision Date: 07/06/1984
Regulation Medical Specialty:
Device Name: DACOMED RIGISCAN SYSTEM
Manufacturer: DACOMED CORP.
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 03/21/1984
Decision Date: 07/06/1984
Regulation Medical Specialty:
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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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