American Diagnostic Corp.
FDA 510(k) & PMA Approved Devices — 39 products
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Total Devices39
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K162589 | Adscope 658 Electronic Stethoscope | DQD | 2017-03-10 | View |
| 510(k) | K093495 | OTOSCOPE AND OPHTHALMOSCOPE DIAGNOSTIC INSTRUMENT KITS | HLJ | 2010-11-19 | View |
| 510(k) | K060321 | ADSCOPE 657BK ELECTRONIC STETHOSCOPE, MODEL 657BK | DQD | 2006-05-15 | View |
| 510(k) | K012304 | ADC 656 ELECTRONIC STETHOSCOPE | DQD | 2001-11-01 | View |
| 510(k) | K962655 | ANEROID AND MERCURIAL SPHYGMOMANOMETERS | DXQ | 1997-01-27 | View |
| 510(k) | K940686 | ELECTRONIC THERMOMETERS | FLL | 1994-07-08 | View |
| 510(k) | K935944 | PROSCOPES AND ADSCOPES | LDE | 1994-03-03 | View |
| 510(k) | K932145 | COAGULATION REFERENCE PLASMA, NORMAL | GIZ | 1993-10-18 | View |
| 510(k) | K894169 | BIOTEL MICROALBUMINURIA (TM) | JIR | 1989-09-18 | View |
| 510(k) | K893608 | ACTICHROME ATIII KIT | JBQ | 1989-06-23 | View |
| 510(k) | K884941 | ACTICLOT C KIT | GGP | 1989-03-13 | View |
| 510(k) | K884940 | RELLPLATE C KIT, RELLPLATE C BULK PLATES | GGP | 1989-03-13 | View |
| 510(k) | K870500 | MAJOR QUALITY GLUCOSE AND KETONES URINE TEST | JIL | 1987-03-06 | View |
| 510(k) | K855239 | BIOTEL (TM)/ DIABETES | JIL | 1986-06-13 | View |
| 510(k) | K855238 | BIOTEL (TM)/UTI | JMT | 1986-05-09 | View |
| 510(k) | K855237 | BIOTEL (TM)/ KIDNEY | KHE | 1986-05-06 | View |
| 510(k) | K832493 | QUINIDINE FLUORESCENT IMMUNOASSAY | LBZ | 1983-09-12 | View |
| 510(k) | K831377 | IGE RADIOIMMUNOASSAY KIT | DGC | 1983-06-02 | View |
| 510(k) | K823062 | KENAMYCIN FLUORESCENT IMMUNOASSAY FIA | KJI | 1982-11-10 | View |
| 510(k) | K822941 | NETILMICIN FLUORESCENT IMMUNOASSAY | LCE | 1982-10-26 | View |
No matching devices.
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