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PROVISC™ Ophthalmic Viscosurgical Device

FDA premarket approval P890047/S061 · decided 2023-08-15

Approval details

PMA number
P890047
Supplement
S061
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
PROVISC™ Ophthalmic Viscosurgical Device
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Alcon Research, Ltd.
Date received
2023-07-20
Decision date
2023-08-15
Days to decision
26 days
Decision code
OK30
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Addition of a redundant Ethylene Oxide (EO) sterilization chamber for routine sterilization of the subject ophthalmic viscosurgical devices.

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510(k) clearances by this applicant

RecordFirmDate
CENTURION Vision System (Active SentryTM) (K161794)Alcon Research, Ltd.2017-04-14
HyperVit Vitrectomy Probe, 23 GA, HyperVit Vitrectomy Probe, 25+, HyperVit Vitrectomy Probe, 27+ (K170520)Alcon Research, Ltd.2017-03-22
CONSTELLATION VISION SYSTEM (K141065)Alcon Research, Ltd.2014-08-22
WAVELIGHT FS200 PATIENT INTERFACE 1505 (K121031)Alcon Research, Ltd.2012-06-21
MONARCH III IOL DELIVERY SYSTEM, MONARCH III C CARTRIDGE, MONARCH III HANDPIECE (H4) (K112977)Alcon Research, Ltd.2012-03-27
27+ ULTRAVIT PROBE, 27+ FLEX-TIP LASER PROBE, 27+ ENDOILLUMINATOR PROBE, 27+ VALVED ENTRY SYSTEM, 27+ INFUSION CANNULA (K110951)Alcon Research, Ltd.2011-10-17
CLEARCUT S SAFETY KNIFE (K110166)Alcon Research, Ltd.2011-05-20
ALCON MULTI-PIRPOSE DISINFECTING SOLUTION (K102860)Alcon Research, Ltd.2011-05-10