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FDA 510(k)

CONTACT LENSES METRO-G 3X (HIOXIFILCON B)

K-Number: K964902 · 1997-03-11

Decision Date1997-03-11
Product CodeLPL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONTACT LENSES METRO-G 3X (HIOXIFILCON B) is the device name listed in this FDA 510(k) record. The listed applicant is Metro Optics of Austin, Inc.. It received FDA 510(k) clearance on 1997-03-11 under 510(k) number K964902. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT LENSES METRO-G 3X (HIOXIFILCON B)?

CONTACT LENSES METRO-G 3X (HIOXIFILCON B) is a medical device that received FDA 510(k) clearance on 1997-03-11. The listed applicant is Metro Optics of Austin, Inc.. The 510(k) number is K964902.

When did CONTACT LENSES METRO-G 3X (HIOXIFILCON B) receive FDA 510(k) clearance?

CONTACT LENSES METRO-G 3X (HIOXIFILCON B) received FDA 510(k) clearance on 1997-03-11, under 510(k) number K964902.

Who is the listed applicant for CONTACT LENSES METRO-G 3X (HIOXIFILCON B)?

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

What is the FDA product code for CONTACT LENSES METRO-G 3X (HIOXIFILCON B)?

The FDA product code for CONTACT LENSES METRO-G 3X (HIOXIFILCON B) is LPL.

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 Metro Optics of Austin, 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: LPL)

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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