Schiller AG
FDA 510(k) & PMA Approved Devices — 17 products
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Total Devices17
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K253562 | medilogFD | MWJ | 2026-08-14 | View |
| 510(k) | K221056 | ARGUS PB-3000 | MHX | 2023-07-06 | View |
| 510(k) | K183425 | CARDIOVIT AT-102 G2 | DPS | 2020-03-02 | View |
| 510(k) | K170182 | CARDIOVIT FT-1 | DPS | 2017-07-19 | View |
| 510(k) | K152043 | Diagnostic Station DS20 | DPS | 2016-05-06 | View |
| 510(k) | K101619 | WELCH ALLYN 1500 PATIENT MONITOR | MHX | 2010-11-12 | View |
| 510(k) | K063814 | BP-200 PLUS | DXN | 2007-03-07 | View |
| 510(k) | K053207 | ARGUS, MODEL LCM | MHX | 2006-05-19 | View |
| 510(k) | K051368 | BR 102 PLUS BLOOD PRESSURE HOLTER SYSTEM | DXN | 2005-08-09 | View |
| 510(k) | K050686 | CARDIOVIT AT-10PLUS | DPS | 2005-05-04 | View |
| 510(k) | K033738 | MONITORING SYSTEM, MODEL ARGUS PB-2200 | DSK | 2004-08-24 | View |
| 510(k) | K031557 | CARDIOVIT AT-102 | DPS | 2004-04-14 | View |
| 510(k) | K012226 | MONITORING SYSTEM,MODEL ARGUS PB-1000 | MHX | 2002-04-08 | View |
| 510(k) | K992823 | SPIROVIT SP-2, PNEUMOCHECK II | BZG | 2000-05-12 | View |
| 510(k) | K984031 | SPIROVIT, MODEL SP-250 | BZG | 1999-04-30 | View |
| 510(k) | K850702 | CARDIOVIT CS-6 ECG-RECORDER | DPS | 1985-04-25 | View |
| 510(k) | K841254 | CARDIOVIT CV-3 | DPS | 1985-01-24 | View |
No matching devices.
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