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EXPANSION OF LATHE LINES FOR INTRAOCULAR LENS MANUFACTURING

FDA premarket approval P080004/S008 · decided 2012-06-13

Approval details

PMA number
P080004
Supplement
S008
Supplement type
135 Review Track For 30-Day Notice
Trade name
EXPANSION OF LATHE LINES FOR INTRAOCULAR LENS MANUFACTURING
Generic name
intraocular lens
Applicant
Hoya Surgical Optics, Inc.
Date received
2011-07-18
Decision date
2012-06-13
Days to decision
331 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Chino Hills, CA
Statement
APPROVAL TO EXPAND INTRAOCULAR LENS MANUFACTURING.

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510(k) clearances by this applicant

RecordFirmDate
HOYA IS INJECTOR SYSTEM (K081346)Hoya Surgical Optics, Inc.2009-03-23