Dacomed Corp.
FDA 510(k) & PMA Approved Devices — 20 products
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Total Devices20
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K953640 | DUNA II PENILE PROSTHESIS | FAE | 1995-10-27 | View |
| 510(k) | K941781 | RIGISCAN PLUS RIGIDITY ASSESSMENT SYSTEM | LIL | 1994-08-25 | View |
| 510(k) | K920409 | DACOMED BATTERY OPERATED VACUUM ERECTION DEVICE | LKY | 1992-05-11 | View |
| 510(k) | K920420 | DURA II PENILE PROSTHESIS | FAE | 1992-04-16 | View |
| 510(k) | K912344 | MODIFIED DURAPHASE(TM) IMPLANTED PENILE PROSTHESIS | FAE | 1991-10-11 | View |
| 510(k) | K900774 | DACOMED NEGATIVE PRESSURE ERECTION DEVICE | LKY | 1990-05-04 | View |
| 510(k) | K885323 | DACOMED EXTERNAL MALE CONTINENCE DEVICE | FHA | 1989-02-08 | View |
| 510(k) | K880391 | DACOMED CYSTOMETER | EXQ | 1988-04-27 | View |
| 510(k) | K871653 | DURAPHASE PENILE PROSTHESIS | FAE | 1987-09-18 | View |
| 510(k) | K870320 | DACOMED PENILE PROSTHESIS SIZER | JLW | 1987-03-17 | View |
| 510(k) | K854118 | DACOMED CORP. ESKA-HERRMAN VOICE PROSTHESIS | EWL | 1986-03-17 | View |
| 510(k) | K850019 | OMNI PHASE PENILE PROSTHESIS | FAE | 1985-04-09 | View |
| 510(k) | K843186 | ESKA MULTISTAGE ESOPHAGEAL BOUGIE | FAT | 1985-01-18 | View |
| 510(k) | K841202 | DACOMED RIGISCAN SYSTEM | LIL | 1984-07-06 | View |
| 510(k) | K834504 | ESKA JONAS SILICON-SILVER PENILE | FAE | 1984-02-04 | View |
| 510(k) | K830667 | SILICONE-SILVER PENILE PROSTHESIS-ESK | FTQ | 1983-10-20 | View |
| 510(k) | K832121 | DACOMED SNAP-GAUGE | LIL | 1983-07-18 | View |
| 510(k) | K820615 | DACOMED SNAP-GAUGE | LIL | 1982-04-21 | View |
| 510(k) | K820081 | ESKA JONAS SILICONE-SILVER PENILE PROST | FAE | 1982-01-25 | View |
| 510(k) | K811693 | FORDER RETRACTOR | KOA | 1981-06-26 | View |
No matching devices.
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