510(K) Premarket Notification
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291 to 300 of 500 Results * |
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|
Device Name
|
Applicant
|
510(K)
Number |
Decision
Date |
---|---|---|---|
dio-dent 10 dental diode laser | MSQ (M2) LTD. | k031819 |
10/30/2003 |
ge logiq 9 ultrasound bt03/iq, model 2375600-x | GE MED. SYSTEMS ULTRASOUND & PRIM. CARE DIAG.,LLC | k032656 |
10/30/2003 |
profusion bone void filler kit | BIOGENERATION | k031838 |
10/30/2003 |
fluid sample retrieval system | BIOMED PERSONAL METABOLIC AND NUTRITIONAL TESTING | k030394 |
10/27/2003 |
ultraflex esophageal ng stent system | BOSTON SCIENTIFIC CORP. | k032930 |
10/23/2003 |
pta balloon catheter | COOK, INC. | k032931 |
10/22/2003 |
autosound 7.6 muscle stimulator, tens, therapeutic ultrasound and combination device | RICH-MAR CORP. | k032941 |
10/22/2003 |
remote access perfusion cannula left axillary 21 french | ESTECH, INC. | k032632 |
10/22/2003 |
linical esoterics calibration verifiers levels a-e for beckman coulter synchron analyzers | CLINIQA CORPORATION | k032074 |
10/21/2003 |
hemedex cranial bolt models, 3601, 3602 | HEMEDEX INCORPORATED | k032337 |
10/21/2003 |
* The maximum 500 records meeting your search criteria returned. Please narrow your search. |
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