Atlas FDA

MONARCH II IOL DELIVERY SYSTEM

FDA 510(k) clearance K001157 · decided 2000-06-27

Clearance details

K-number
K001157
Device name
MONARCH II IOL DELIVERY SYSTEM
Applicant
Alcon Research, Ltd.
Decision
Substantially Equivalent
Date received
2000-04-10
Decision date
2000-06-27
Days to decision
78 days
Clearance type
Traditional
Product code
KYB
Device class
1
Regulation number
886.4300
Medical specialty
Ophthalmic
Advisory committee
Ophthalmic
Location
Fort Worth, TX, US
Third-party review
No
Expedited review
No

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RE-USEABLE MICROSTAAR INJECTOR, MSI-S (K032412)Staar Surgical Co.2004-06-10
MASTEL 1 FOLDER IMPLANTATION SYSTEM (K022723)Mastel Precision, Inc.2002-12-26
DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1) (K983129)Staar Surgical Co.1998-12-04
MONARCH IOL DELIVERY SYSTEM (K981571)Alcon Laboratories1998-07-09
MONARCH IOL DELIVERY SYSTEM (K970033)Alcon Laboratories1997-04-23
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Recalls involving this device

RecordFirmDate
MONARCH II IOL Delivery System, Cartridge Model B, part #8065977758, packaged in pouches, recall (Z-2441-2008)Alcon Laboratories, Inc2008-09-23

PMA approvals by this applicant

RecordFirmDate
AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses (P040020/S117)Alcon Research, Ltd.2025-12-12
PROVISC™ Ophthalmic Viscosurgical Device (P890047/S069)Alcon Research, Ltd.2025-10-03
AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses (P040020/S116)Alcon Research, Ltd.2025-09-18
AcrySof® IQ ReSTOR® Posterior Chamber Intraocular Lenses\s (P040020/S115)Alcon Research, Ltd.2025-08-25
PROVISC™ Ophthalmic Viscosurgical Device (P890047/S068)Alcon Research, Ltd.2025-07-25
AcrySof IQ ReSTOR Posterior Chamber Intraocular Lenses (P040020/S111)Alcon Research, Ltd.2025-06-18
PROVSIC Ophthalmic Viscosurgical Device (P890047/S067)Alcon Research, Ltd.2025-02-26
AcrySof ReSTOR Posterior Chamber Intraocular Lens (IOL) (P040020/S113)Alcon Research, Ltd.2025-02-14