Medical Device Manufacturer · US , South Natick , MA

Harvard Clinical Technology - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Harvard Clinical Technology has 2 FDA 510(k) cleared medical devices. Based in South Natick, US.

Historical record: 2 cleared submissions from 2003 to 2005. Primary specialty: General Hospital.

Browse the FDA 510(k) cleared devices submitted by Harvard Clinical Technology Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Harvard Clinical Technology

2 devices
1-2 of 2
Cleared Feb 11, 2005
HARVARD 2 SYRINGE PUMP, MODEL 2001-001
K050107 · FRN
General Hospital · 24d
Cleared Dec 16, 2003
HARVARD 1 SYRINGE PUMP/HARVARD 1 WITH PCA SYRINGE PUMP
K033054 · MEA
General Hospital · 78d
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