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FDA 510(k), K941781, RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
FDA 510(k), K941781, RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
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510(K) Number: K941781
Device Name: RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
Manufacturer: DACOMED CORP.
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 04/11/1994
Decision Date: 08/25/1994
Regulation Medical Specialty:
Device Name: RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
Manufacturer: DACOMED CORP.
Device Classification Name: monitor, penile tumescence
Regulation Number:
Classification Product Code: LIL
Date Received: 04/11/1994
Decision Date: 08/25/1994
Regulation Medical Specialty:
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- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
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