Dacomed Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Dacomed Corp. - FDA 510(k) Cleared Devices
20
Total
20
Cleared
0
Denied
Dacomed Corp. has 20 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 20 cleared submissions from 1981 to 1995.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Dacomed Corp.
20 devices
Cleared
Oct 27, 1995
DUNA II PENILE PROSTHESIS
Gastroenterology & Urology
84d
Cleared
Aug 25, 1994
RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM
Gastroenterology & Urology
136d
Cleared
May 11, 1992
DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE
Gastroenterology & Urology
101d
Cleared
Apr 16, 1992
DURA II PENILE PROSTHESIS
Gastroenterology & Urology
76d
Cleared
Oct 11, 1991
MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS
Gastroenterology & Urology
136d
Cleared
May 04, 1990
DACOMED NEGATIVE PRESSURE ERECTION DEVICE
Gastroenterology & Urology
73d
Cleared
Feb 08, 1989
DACOMED EXTERNAL MALE CONTINENCE DEVICE
Gastroenterology & Urology
42d
Cleared
Apr 27, 1988
DACOMED CYSTOMETER
Gastroenterology & Urology
89d
Cleared
Sep 18, 1987
DURAPHASE PENILE PROSTHESIS
Gastroenterology & Urology
143d
Cleared
Mar 17, 1987
DACOMED PENILE PROSTHESIS SIZER
Chemistry
48d
Cleared
Mar 17, 1986
DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS
Ear, Nose, Throat
159d
Cleared
Apr 09, 1985
OMNI PHASE PENILE PROSTHESIS
Gastroenterology & Urology
96d