Atlas FDA

COBURN(R) POSTERIOR INTRAOCULAR LENSES

FDA premarket approval P860002/S006 · decided 1990-11-15

Approval details

PMA number
P860002
Supplement
S006
Supplement type
Normal 180 Day Track
Supplement reason
Other
Trade name
COBURN(R) POSTERIOR INTRAOCULAR LENSES
Generic name
intraocular lens
Applicant
Bausch & Lomb
Date received
1990-10-23
Decision date
1990-11-15
Days to decision
23 days
Decision code
APPR
Product code
HQL
Advisory committee
Ophthalmic
Expedited review
No
Location
Rochester, NY

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Stellaris Elite vision enhancement system (K170052)Bausch+Lomb2017-04-19
Stellaris Elite Vision Enhancement System (K162342)Bausch+Lomb2017-03-24
STELLARIS PC VISION ENHANCEMENT SYSTEM (K133486)Bausch & Lomb2014-03-12
STELLARIS VISION ENHANCEMENT SYSTEM (K133242)Bausch & Lomb2014-02-14
BAUSCH & LOMB INJECTOR SYSTEM (K131958)Bausch & Lomb2014-01-09
BAUSCH + LUMB, VIS100 INJECTOR SYSTEM (K133146)Bausch & Lomb2014-01-03
EASY-LOAD LENS DELIVERY SYSTEM (K132481)Bausch & Lomb2013-12-27
CRYSTALSERT DELIVERY SYSTEM (K132593)Bausch & Lomb2013-09-17