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FDA 510(k)

VITRECTOMY CUTTER AND ACCESSORIES

K-Number: K081681 · 2008-10-08

Decision Date2008-10-08
Product CodeMLZ
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

VITRECTOMY CUTTER AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Medical Optics, Inc.. It received FDA 510(k) clearance on 2008-10-08 under 510(k) number K081681. The device is classified under product code MLZ. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VITRECTOMY CUTTER AND ACCESSORIES?

VITRECTOMY CUTTER AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 2008-10-08. The listed applicant is Advanced Medical Optics, Inc.. The 510(k) number is K081681.

When did VITRECTOMY CUTTER AND ACCESSORIES receive FDA 510(k) clearance?

VITRECTOMY CUTTER AND ACCESSORIES received FDA 510(k) clearance on 2008-10-08, under 510(k) number K081681.

Who is the listed applicant for VITRECTOMY CUTTER AND ACCESSORIES?

The FDA 510(k) record lists Advanced Medical Optics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITRECTOMY CUTTER AND ACCESSORIES?

The FDA product code for VITRECTOMY CUTTER AND ACCESSORIES is MLZ.

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.

Other records listing Advanced Medical Optics, Inc. 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.

View all 8 devices →

Related Devices (Code: MLZ)

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

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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