Medical Device Manufacturer · US , Morrisville , NC

Sicel Technologies, Inc. - FDA 510(k) Cleared Devices

7 submissions · 7 cleared · Since 2004
7
Total
7
Cleared
0
Denied

Sicel Technologies, Inc. has 7 FDA 510(k) cleared medical devices. Based in Morrisville, US.

Historical record: 7 cleared submissions from 2004 to 2008. Primary specialty: Radiology.

Browse the FDA 510(k) cleared devices submitted by Sicel Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Sicel Technologies, Inc.
7 devices
1-7 of 7
Cleared Nov 13, 2008
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM
K083035 · NZT
Radiology · 30d
Cleared Aug 04, 2008
MODIFICATION TO ONEDOSE PATIENT DOSIMETRY SYSTEM
K081859 · IYE
Radiology · 34d
Cleared Jan 23, 2008
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM
K080004 · NZT
Radiology · 21d
Cleared Jun 20, 2007
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODEL DVS-I-11: DVS...
K071399 · LHN
Radiology · 30d
Cleared Jun 13, 2006
DOSE VERIFICATION SYSTEM PATIENT DOSIMETRY SYSTEM, MODELS DVS-I-11, DVS...
K061051 · LHN
Radiology · 57d
Cleared Apr 03, 2006
DOSE VERIFICATION SYSTEM
K052118 · LHN
Radiology · 242d
Cleared Jun 25, 2004
ONEDOSE PATIENT DOSIMETRY SYSTEM
K040687 · IYE
Radiology · 101d
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