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PROVISC™ Ophthalmic Viscosurgical Device

FDA premarket approval P890047/S060 · decided 2023-03-29

Approval details

PMA number
P890047
Supplement
S060
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
2023-03-10
Decision date
2023-03-29
Days to decision
19 days
Decision code
OK30
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Fort Worth, TX
Statement
Reduction in the aeration phase of your existing approved Ethylene Oxide sterilization process.

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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