FDA 510(k) Applications Submitted by SICEL TECHNOLOGIES, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K081859 |
07/01/2008 |
MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM |
SICEL TECHNOLOGIES, INC. |
| K083035 |
10/14/2008 |
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM |
SICEL TECHNOLOGIES, INC. |
| K080004 |
01/02/2008 |
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM |
SICEL TECHNOLOGIES, INC. |
| K061051 |
04/17/2006 |
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODELS DVS-I-11, DVS INSERTION TOOL, DVS-D-A, DVS DOSIMETER |
SICEL TECHNOLOGIES, INC. |
| K071399 |
05/21/2007 |
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODEL DVS-I-11: DVS INSERTION TOOL, DVS-D-A: DVS DOSIMETER, DVS-R-100 |
SICEL TECHNOLOGIES, INC. |
| K052118 |
08/04/2005 |
DOSE VERIFICATION SYSTEM |
SICEL TECHNOLOGIES, INC. |
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