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FDA 510(k)

MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM

K-Number: K073591 · 2008-03-13

ApplicantStaar Surgical Co.
Decision Date2008-03-13
Product CodeMSS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Staar Surgical Co.. It received FDA 510(k) clearance on 2008-03-13 under 510(k) number K073591. The device is classified under product code MSS. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM?

MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM is a medical device that received FDA 510(k) clearance on 2008-03-13. The listed applicant is Staar Surgical Co.. The 510(k) number is K073591.

When did MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM receive FDA 510(k) clearance?

MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM received FDA 510(k) clearance on 2008-03-13, under 510(k) number K073591.

Who is the listed applicant for MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM?

The FDA 510(k) record lists Staar Surgical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM?

The FDA product code for MICROSTAAR MSI INJECTOR FOAM TIP SYSTEM is MSS.

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Other records listing Staar Surgical Co. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K090161EPIPHANY INJECTION SYSTEMK073586MICROSTAAR INDIGO INJECTOR FOAM TIP SYSTEMK032412RE-USEABLE MICROSTAAR INJECTOR, MSI-SK020734SURGE-FREE ASPIRATION ADAPTERK983129DISPOSABLE MICROSTAAR INJECTOR (MODEL MSI-P1)K980696FOAM TIP INJECTOR

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Related Devices (Code: MSS)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K261174RxSight® Insertion DeviceRxsight, Inc.K252540ACCUJECT Injector Set 2.1-1P (LP604590)Medicel AGK242389EyeGility™ Inserter for Preloaded enVista IOLsBausch & Lomb, IncorporatedK231106Accuject Refra Injector AR2900Medicel AGK231838RxSight® Insertion Device (63002)Rxsight, Inc.K231466RxSight Insertion DeviceRxsight, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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