Search
Companies
Product Codes
Device Names
Contacts
Applications
Decisions
Contact
FDA 510(k) Application Details - K132593
Device Classification Name
Folders And Injectors, Intraocular Lens (Iol)
More FDA Info for this Device
510(K) Number
K132593
Device Name
Folders And Injectors, Intraocular Lens (Iol)
Applicant
BAUSCH & LOMB
30 ENTERPRISE, SUITE 450
ALISO VIEJO, CA 92656-7115 US
Other 510(k) Applications for this Company
Contact
YI GAO
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
08/19/2013
Decision Date
09/17/2013
Decision
SESE - SUBST EQUIV
Classification Advisory Committee
OP - Ophthalmic
Review Advisory Committee
OP - Ophthalmic
Statement / Summary / Purged Status
Summary
Type
Special
Reviewed By Third Party
N
Expedited Review
Search
|
Companies
|
Product Codes
|
Device Names
|
Contacts
|
Applications
|
Decisions
|
Contact