FDA 510(k) Applications Submitted by ORIGIN MEDSYSTEMS, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K955163 |
11/13/1995 |
DISSECTION PROBE |
ORIGIN MEDSYSTEMS, INC. |
K960637 |
02/14/1996 |
5MM ENDOSCOPE |
ORIGIN MEDSYSTEMS, INC. |
K970611 |
02/18/1997 |
ORIGIN CARDIAC STABLIZER OCCLUDER |
ORIGIN MEDSYSTEMS, INC. |
K960936 |
03/08/1996 |
RESPOSABLE TROCAR SYSTEM [5MM, 5MM SHORT, 10MM AND 12MM SIZES] |
ORIGIN MEDSYSTEMS, INC. |
K962005 |
05/22/1996 |
EXTRAHAND BALLOON RETRACTOR |
ORIGIN MEDSYSTEMS, INC. |
K962104 |
05/30/1996 |
AIRLIFT BALLOON RETRACTON SYSTEM |
ORIGIN MEDSYSTEMS, INC. |
K972685 |
07/17/1997 |
ORIGIN LIGATOR DEVICE |
ORIGIN MEDSYSTEMS, INC. |
K964171 |
10/18/1996 |
VASOVIEW BALLOON DISSECTION SYSTEM |
ORIGIN MEDSYSTEMS, INC. |
K965121 |
12/23/1996 |
CANNULA |
ORIGIN MEDSYSTEMS, INC. |
K981700 |
05/14/1998 |
VASOVIEW DISSECTION/VESSEL HARVESTING SYSTEM |
ORIGIN MEDSYSTEMS, INC. |
K992353 |
07/14/1999 |
BLUNT TIP TROCAR PORT |
ORIGIN MEDSYSTEMS, INC. |
|
|