FDA 510(k) Applications Submitted by DAVID MAKANANI
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980869 |
03/06/1998 |
SYNOX SX 53-BP, SX 60-BP, SX 45-JBP, SX 53-JBP , MODELS 120 444, 119 684, 120 438 AND 120 143 |
BIOTRONIK, INC. |
| K982272 |
06/29/1998 |
GALEO HS 014 MODEL 117 130, GALEO S 014 MODEL 115 488, GALEAO M 014 MODEL 114156, GALEO F 014 MODEL 115 487 GALEO HF 018 |
BIOTRONIK, INC. |
| K072499 |
09/05/2007 |
NOVOFLO CATHETER LT |
NOVOSCI, INC. |
| K063355 |
11/07/2006 |
D-LINE CATHETER ST, DOUBLE LUMEN ST; EXTRA FLOW |
NOVOSCI CORP. |
| K960169 |
01/16/1996 |
CARBOMEDICS VALVE TESTER |
CARBOMEDICS, INC. |
| K960923 |
03/06/1996 |
CARBOMEDICS MITRAL ROTATOR |
CARBOMEDICS, INC. |
|
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