Company ยท US
Harvest Technologies, Corp.
FDA 510(k) clearances and medical device recalls filed under this name, 1999 to 2012. Name variants (Inc, Corp, punctuation) are merged.
9510(k) clearances (0 in 12 months)
1recalls (0 in 12 months)
1recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Sep 21, 2012 | K121005 | ADIPREP ADIPOSE TRANSFER SYSTEM Harvest Technologies, Corp. | MUU |
| Dec 6, 2010 | K103340 | SMARTPREP2 BMAC SYSTEM, SMARTPREP PLATELET CONCENTRATION SYSTEM Harvest Technologies, Corp. | JQC |
| Jan 4, 2006 | K052925 | SMARTPREP2 CENTRIFUGE SYSTEM Harvest Technologies, Corp. | JQC |
| Mar 11, 2005 | K043261 | HARVEST GRAFT DELIVERY SYRINGE Harvest Technologies, Corp. | FMF |
| Apr 5, 2002 | K020252 | SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 Harvest Technologies, Corp. | FMF |
| Jul 3, 2001 | K011032 | SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE GRAFT LIQUID APPLICATOR (DUAL LUMEN CANNULA Harvest Technologies, Corp. | LYC |
| Jun 1, 2000 | K000456 | HARVEST TECHNOLOGIES DUAL LIQUID APPLICATOR, MODEL SK/S: HARVEST DUAL LIQUID APPLICATOR LK/2 Harvest Technologies, LLC | FMF |
| May 28, 1999 | K991430 | SMARTPREP CENTRIFUGE SYSTEM Harvest Technologies, LLC | JQC |
| Apr 2, 1999 | K983022 | SMARTCELL PROCESSING SYSTEM Harvest Technologies, LLC | CAC |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Oct 17, 2013 | Harvest Technologies Corporation Harvest Graft Delivery System; Model Number: GDP-10
Product Usage: The Harvest Graft Delivery System is intended for the aspiration of bone marrow, autologous blood, plasma, or other body fluids. Th Terminated |
FMF | K043261 |