FDA 510(k) Applications Submitted by CARL BEAURLINE
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K061516 |
06/01/2006 |
STAODYN MAX PRESET, MODEL 4470 |
COMPEX TECHNOLOGIES, INC. |
K061650 |
06/13/2006 |
SELECT TENS, MODEL 4600S |
EMPI |
K133502 |
11/14/2013 |
5000Z FIREFLY SYSTEM |
PRIZM MEDICAL, INC. |
K000013 |
01/03/2000 |
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R-2000 |
ACIST MEDICAL SYSTEMS |
K010390 |
02/09/2001 |
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL R2000-CMS |
ACIST MEDICAL SYSTEMS, INC. |
K040298 |
02/09/2004 |
ACIST ANTIOGRAPHIC INJECTION SYSTEM CONTRAST MANAGEMENT DISPOSABLE KITS |
ACIST MEDICAL SYSTEMS, INC. |
K020892 |
03/19/2002 |
ACIST GENTOO CONTRAST INJECTION SYSTEM |
ACIST MEDICAL SYSTEMS |
K021015 |
03/29/2002 |
ACIST PLUS 4 ANGIOGRAPHIC CATHETER |
ACIST MEDICAL SYSTEMS |
K991103 |
04/01/1999 |
MODIFICATION TO ACIST CL 100H |
ACIST MEDICAL SYSTEMS |
K060941 |
04/06/2006 |
CAAS MRV VERSION 3.0 |
PIE MEDICAL IMAGING B.V. |
K012983 |
09/05/2001 |
ACIST 4 FRENCH ANGIOGRAPHIC CATHETER |
ACIST MEDICAL SYSTEMS, INC. |
K993774 |
11/08/1999 |
ACIST ANGIOGRAPHIC INJECTION SYSTEM, MODEL CL1OOH |
ACIST MEDICAL SYSTEMS |
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