FDA 510(k) Applications Submitted by DUCKWORTH & KENT, LTD.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K060995 |
04/11/2006 |
DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788 |
DUCKWORTH & KENT, LTD. |
| K081382 |
05/16/2008 |
DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 |
DUCKWORTH & KENT, LTD. |
| K042478 |
09/13/2004 |
CAPSULE TENSION RING INSERTER, MODEL 7-810 |
DUCKWORTH & KENT, LTD. |
| K072985 |
10/23/2007 |
DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 |
DUCKWORTH & KENT, LTD. |
| K053176 |
11/14/2005 |
DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797 |
DUCKWORTH & KENT, LTD. |
| K024072 |
12/10/2002 |
DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM |
DUCKWORTH & KENT, LTD. |
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