Atlas FDA

SOFTEC INTRAOCULAR LENSES (IOLS)

FDA premarket approval P090022/S021 · decided 2014-04-17

Approval details

PMA number
P090022
Supplement
S021
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
SOFTEC INTRAOCULAR LENSES (IOLS)
Generic name
intraocular lens
Applicant
Lenstec, Inc.
Date received
2014-03-19
Decision date
2014-04-17
Days to decision
29 days
Decision code
OK30
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
St. Petersburg, FL
Statement
ADDITION OF A STEAM STERILIZER.

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510(k) clearances by this applicant

RecordFirmDate
Lenstec LC Injection system (K161776)Lenstec, Inc.2016-11-29
LENSTEC LC INJECTION SYSTEM (K122848)Lenstec, Inc.2013-10-18
FLUID ISOLATION DEVICE (K091915)Lenstec, Inc.2009-10-27
LENSTEC LC INJECTION SYSTEM (K063802)Lenstec, Inc.2007-05-07
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM (K060533)Lenstec, Inc.2006-04-14
LENSTEC INTRAOCULAR LENS (IOL) INJECTION SYSTEM FOR TETRAFLEX INTRAOCULAR LENSES (K050638)Lenstec, Inc.2005-05-31