Company ยท GB
Duckworth & Kent, Ltd.
FDA 510(k) clearances and medical device recalls filed under this name, 2003 to 2008. Name variants (Inc, Corp, punctuation) are merged.
6510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)
Product codes
Latest 510(k) clearances
| Decided | 510(k) | Device and applicant | Code |
|---|---|---|---|
| Oct 23, 2008 | K081382 | DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786 Duckworth & Kent, Ltd., GB | KYB |
| Jun 20, 2008 | K072985 | DUCKWORTH & KENT LTD INJECTOR, MODEL: DK7797-2 Duckworth & Kent, Ltd., GB | KYB |
| May 22, 2006 | K060995 | DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM, MODEL DK7788 Duckworth & Kent, Ltd., GB | MSS |
| Jan 30, 2006 | K053176 | DUCKWORTH & KENT LTD CARTRIDGE LENS DELIVERY SYSTEM, MODEL DK7797 Duckworth & Kent, Ltd., GB | MSS |
| Dec 28, 2004 | K042478 | CAPSULE TENSION RING INSERTER, MODEL 7-810 Duckworth & Kent, Ltd., GB | NCE |
| Oct 6, 2003 | K024072 | DUCKWORTH & KENT LTD LENS DELIVERY SYSTEM Duckworth & Kent, Ltd., GB | MSS |
Latest recalls
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| No recalls in this window. | |||