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FDA 510(k) K841202, DACOMED RIGISCAN SYSTEM, by Dacomed Corp.

FDA 510(k) K841202, DACOMED RIGISCAN SYSTEM, by Dacomed Corp.

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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

Total pages: 91
Fully redacted pages: 24
Content pages: 67

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