Critikon Company, LLC
FDA 510(k) & PMA Approved Devices — 51 products
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Total Devices51
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K002248 | DINAMAP PRO 1000 MONITOR, MODEL 1000 | DXN | 2000-09-21 | View |
| 510(k) | K000500 | DINAMAP ADVANCED NIBP MODULE | DXN | 2000-05-26 | View |
| 510(k) | K992638 | DINAMAP PRO SERIES MONITOR, MODELS 100, 200, 300, 400 | MWI | 2000-02-24 | View |
| 510(k) | K982342 | DINAMAP MPS SELECT PORTABLE MONITOR | MSX | 1998-08-14 | View |
| 510(k) | K943709 | DINAMAP PLUS VITAL SIGNS MONOITOR | DPS | 1995-06-16 | View |
| 510(k) | K942700 | DINAMAP VITAL SIGNS MONITOR MODELS 9300 AND 9320/9340 | MHX | 1995-03-01 | View |
| 510(k) | K933404 | CRITIKON CENTRAL STATIN MONITOR | DPS | 1994-02-09 | View |
| 510(k) | K933050 | CHANGES TO PROTECTIV(TM) & JELCO(TM) WINGED CATH | FOZ | 1993-12-14 | View |
| 510(k) | K915697 | CRITIKON VITAL SIGNS MODULE | DXN | 1993-07-01 | View |
| 510(k) | K921295 | INTRAVENOUS CATHETERS MODIFICATIONS | FGO | 1993-05-17 | View |
| 510(k) | K912188 | DINAMAP PLUS PHYSIOLOGICAL MONITOR MODEL 8700 | MHX | 1991-12-04 | View |
| 510(k) | K911769 | RATEMINDER(TM) V INFUSION PUMP, MODIFICATION | FRN | 1991-06-03 | View |
| 510(k) | K902092 | RATEMINDER V INFUSION PUMP W/SECONDARY CAPABILITY | FRN | 1990-07-26 | View |
| 510(k) | K894100 | OXYTRAK(TM) PULSE OXIMETER | DQA | 1990-05-09 | View |
| 510(k) | K893546 | OPTICALLY CLEAR RADIOPAQUE CATHETER | FOZ | 1989-11-01 | View |
| 510(k) | K874546 | SIM MODULE | FRN | 1988-05-11 | View |
| 510(k) | K875174 | RATEMINDER V INFUSION PUMP | FRN | 1988-03-29 | View |
| 510(k) | K874442 | DINAMAP VITAL SIGNS MONITOR/PULSE OXIMETER | DQA | 1988-02-18 | View |
| 510(k) | K875177 | J&J SCALP VEIN INFUSION SETS | FOZ | 1988-01-14 | View |
| 510(k) | K874378 | DINAMAP VITAL SIGNS MONITOR, MODEL 8100T | DXN | 1987-12-30 | View |
No matching devices.
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