FDA 510(k), K841202, DACOMED RIGISCAN SYSTEM

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