Medical Device Consultants, Inc.
FDA 510(k) & PMA Approved Devices — 14 products
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Total Devices14
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K022895 | ELCAM STOPCOCKS AND MANIFOLDS | FMG | 2002-10-18 | View |
| 510(k) | K002699 | PARIETEX COMPOSITE (PCO) MESH | FTL | 2001-02-15 | View |
| 510(k) | K002116 | S3 CARDIOPLEGIA CONTROL MODULE VERSION 2.0 | DTQ | 2000-08-09 | View |
| 510(k) | K000551 | IMAGE X-70 PLUS DENTAL X-RAY UNIT | EHD | 2000-03-16 | View |
| 510(k) | K974164 | SWISS LITHOCLAST MASTER HANDPIECE AND 3.2 MM PROBE | FFK | 1997-12-18 | View |
| 510(k) | K864282 | GLUCOSE TESTCARD USE W/ILEX PROMPT CLINICAL CH ANA | CGA | 1987-05-26 | View |
| 510(k) | K860122 | HEMOTEC ACT HIGH RANGE ACTIVATED CLOTTING TIME | JBP | 1986-04-04 | View |
| 510(k) | K860929 | ULTRASUN 4000 FT & 15000-8 SUNTANNING UNIT | FTC | 1986-03-28 | View |
| 510(k) | K860930 | ULTRASUN 2500 SUNTANNING UNIT | FTC | 1986-03-28 | View |
| 510(k) | K860932 | ULTRASUN 1000 & 2000 SUNTANNING UNIT | FTC | 1986-03-28 | View |
| 510(k) | K860931 | ULTRASUN 3000 AND 5000 SUNTANNING UNIT | FTC | 1986-03-28 | View |
| 510(k) | K853198 | ADDITIONAL HEMOTEC ACT COAGULATION CARTRIDGES | JPA | 1985-10-04 | View |
| 510(k) | K840449 | AMICON DIAFILTER 40. HEMOFILTER | KDI | 1984-03-23 | View |
| 510(k) | K821651 | E-Z UP ARTHERAPEDIC CHAIR | INN | 1982-06-24 | View |
No matching devices.
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