Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K024072
Device Classification Name
Folders And Injectors, Intraocular Lens (Iol)
More FDA Info for this Device
510(K) Number
K024072
Device Name
Folders And Injectors, Intraocular Lens (Iol)
Applicant
DUCKWORTH & KENT, LTD.
7 MARQUIS BUSINESS CENTRE
ROYSTON RD.
BALDOCK, HERTSFORDSHIRE SG7 6XL GB
Other 510(k) Applications for this Company
Contact
MARTIN LOCK
Other 510(k) Applications for this Contact
Regulation Number
886.4300
More FDA Info for this Regulation Number
Classification Product Code
MSS
Other 510(k) Applications for this Device
More FDA Info for this Product Code
Date Received
12/10/2002
Decision Date
10/06/2003
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Statement
Type
Traditional
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact