Analogic Corp.
FDA 510(k) & PMA Approved Devices — 32 products
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Total Devices32
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K071430 | SYNERAD OMNI, MODELS AN6255 AND AN6265 | KPR | 2007-06-21 | View |
| 510(k) | K052447 | SYNERAD IMPACT 60, SYNERAD IMPACT 72 AND ANALOGIC AMS1600 | JAK | 2005-09-21 | View |
| 510(k) | K050919 | LIFEGARD II FAMILY MULTI-FUNCTION PATIENT MONITOR, MODELS AN4320, AN4320P, AN4321P, AN4322P & AN3423P | DSI | 2005-06-14 | View |
| 510(k) | K043025 | SYNERAD OMNI, DIGITAL X-RAY SYSTEM, MODEL AN6250 | KPR | 2004-11-19 | View |
| 510(k) | K041434 | C3 AND LIFEGARD ICG IMPEDANCE CARDIOGRAPHY MONITORS | DSB | 2004-08-06 | View |
| 510(k) | K041376 | C1 SERIES PATIENT MONITOR, MODELS 863051, 863052, 863053, 863054; OPTIONAL PRINTER FOR CI, MODEL M3925A | MWI | 2004-07-20 | View |
| 510(k) | K040995 | SYNERAD MULTI DIGITAL X-RAY SYSTEM, MODEL AN6150 | KPR | 2004-05-25 | View |
| 510(k) | K033345 | AN5150 AND AN7150 DIGITAL RADIOLOGY SYSTEMS | KPR | 2003-11-19 | View |
| 510(k) | K030931 | C3 PATIENT MONITOR | MHX | 2003-05-09 | View |
| 510(k) | K011304 | OB-1 FETAL MONITOR | HGM | 2001-05-29 | View |
| 510(k) | K002503 | FETALGARD LITE | HGM | 2000-11-09 | View |
| 510(k) | K001336 | DR9000 DIGITAL RADIOGRAPHY X-RAY SYSTEM | KPR | 2000-06-02 | View |
| 510(k) | K001341 | DR5000 DEDICATED CHEST X-RAY SYSTEM | KPR | 2000-06-02 | View |
| 510(k) | K983395 | FETALGARD 3000 FETAL MONITOR | HGM | 1999-08-12 | View |
| 510(k) | K991626 | WEBRAD COMPUTED RADIOGRAPHY QUALITY ASSURANCE WORKSTATION | LLZ | 1999-07-02 | View |
| 510(k) | K980411 | NPB3900 SERIES PATIENT MONITORS | MHX | 1998-08-20 | View |
| 510(k) | K980168 | COMPUTED RADIOGRAPHY QUALITY ASSURANCE SOFTWARE | LLZ | 1998-04-02 | View |
| 510(k) | K974455 | ANATOM 1000 (A MINUS, A-) | JAK | 1998-02-20 | View |
| 510(k) | K964890 | ANATOM 2000 | JAK | 1997-03-06 | View |
| 510(k) | K962424 | NPB-4000 | MHX | 1996-12-20 | View |
No matching devices.
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