Harvest Technologies, Corp. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Harvest Technologies, Corp. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Harvest Technologies, Corp. has 6 FDA 510(k) cleared medical devices. Based in Plymouth, US.
Historical record: 6 cleared submissions from 2001 to 2012.
Browse the FDA 510(k) cleared devices submitted by Harvest Technologies, Corp. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Harvest Technologies, Corp.
6 devices
Cleared
Sep 21, 2012
ADIPREP ADIPOSE TRANSFER SYSTEM
General & Plastic Surgery
171d
Cleared
Dec 06, 2010
SMARTPREP2 BMAC SYSTEM, SMARTPREP PLATELET CONCENTRATION SYSTEM
Hematology
21d
Cleared
Jan 04, 2006
SMARTPREP2 CENTRIFUGE SYSTEM
Hematology
78d
Cleared
Mar 11, 2005
HARVEST GRAFT DELIVERY SYRINGE
General Hospital
107d
Cleared
Apr 05, 2002
SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2
General Hospital
71d
Cleared
Jul 03, 2001
SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE...
Dental
89d