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FDA 510(k)

MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER

K-Number: K011392 · 2001-10-22

Decision Date2001-10-22
Product CodeMSS
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER is the device name listed in this FDA 510(k) record. The listed applicant is Micra Instruments. It received FDA 510(k) clearance on 2001-10-22 under 510(k) number K011392. 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 MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER?

MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER is a medical device that received FDA 510(k) clearance on 2001-10-22. The listed applicant is Micra Instruments. The 510(k) number is K011392.

When did MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER receive FDA 510(k) clearance?

MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER received FDA 510(k) clearance on 2001-10-22, under 510(k) number K011392.

Who is the listed applicant for MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER?

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

What is the FDA product code for MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER?

The FDA product code for MICRA LENS INJECTOR, MICRA CARTRIDGE LENS, MICRA LENS LOADER is MSS.

Related Clinical Trials

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.

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.

Official Source

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

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