510(K) Premarket Notification
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311 to 320 of 500 Results * |
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|
Device Name
|
Applicant
|
510(K)
Number |
Decision
Date |
---|---|---|---|
gynecare prolene fastener system | ETHICON, INC. | k042603 |
12/22/2004 |
endorez | ULTRADENT PRODUCTS, INC. | k042756 |
10/26/2004 |
needle incapacitator (needle guard) | PDMP, INC. | k042907 |
12/22/2004 |
randox phencyclidine assay | RANDOX LABORATORIES, LTD. | k043071 |
01/27/2005 |
dragon heart i.v. set | DRAGON HEART MEDICAL DEVICES CO., LTD. | k043235 |
03/08/2005 |
reprocessed ep technologies electrophysiology catheters | ALLIANCE MEDICAL CORP. | k043393 |
03/23/2005 |
medela dominant 35 c/i secretion and surgical aspirator | MEDELA AG | k043544 |
01/07/2005 |
complete brand multi-purpose solution | ADVANCED MEDICAL OPTICS, INC. | k030092 |
04/04/2003 |
freezor xtra surgical cardiac cryoablation device and cct.2 cardiac cardiac cryoablation cryoconsole | CRYOCATH TECHNOLOGIES, INC. | k030303 |
04/29/2003 |
oria zenith | ORTHOTEC, L.L.C. | k030500 |
03/20/2003 |
* The maximum 500 records meeting your search criteria returned. Please narrow your search. |
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