DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786


Device Classification Name

lens, guide, intraocular

510(k) Number K081382
Device Name DUCKWORTH & KENT, LTD., IMPLANTATION SYSTEM, MODEL DK7786
Applicant
DUCKWORTH & KENT, LTD.
7 marquis business centre
royston rd.
baldock, hertsfordshire, 

GB

sg7 6xl

Applicant Contact martin lock
Correspondent
DUCKWORTH & KENT, LTD.
7 marquis business centre
royston rd.
baldock, hertsfordshire, 

GB

sg7 6xl

Correspodent Contact martin lock
Regulation Number 886.4300
Classification Product Code
KYB  
Date Received 05/16/2008
Decision Date 10/23/2008
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Ophthalmic

510k Review Panel

Ophthalmic

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No