Harvard Clinical Technology is one of 23810 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Harvard Clinical Technology - FDA 510(k) Cleared Devices
Recent clearances: HARVARD 2 SYRINGE PUMP, MODEL 2001-001, HARVARD 1 SYRINGE PUMP/HARVARD 1 WITH PCA SYRINGE PUMP
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.
510(k) submissions have been managed by Underwriters Laboratories, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Harvard Clinical Technology
2 devices