FDA 510(k) Applications Submitted by WUESTEC MEDICAL, INC.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K992103 |
06/22/1999 |
C-QUEST |
WUESTEC MEDICAL, INC. |
K992603 |
08/03/1999 |
XRT 600 R/F, WRF 0600 |
WUESTEC MEDICAL, INC. |
K993962 |
10/25/1999 |
PENSIL TRAUMA, MODEL WWS6100 |
WUESTEC MEDICAL, INC. |
K981880 |
05/28/1998 |
DX-480, ADD ON DIGITAL IMAGER |
WUESTEC MEDICAL, INC. |
K960083 |
01/11/1996 |
MOVABLE CANTILEVERED RADIOGRAPHIC TABLE XRT 100, 200 & 300 |
WUESTEC MEDICAL, INC. |
K955414 |
11/27/1995 |
XRT 400 |
WUESTEC MEDICAL, INC. |
K974240 |
11/12/1997 |
LIGHTLINE-M |
WUESTEC MEDICAL, INC. |
K935123 |
10/28/1993 |
SUPERSTAND 300 |
WUESTEC MEDICAL, INC. |
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