CONTACT LENSES METRO-G 3X (HIOXIFILCON B)
K-Number: K964902 · 1997-03-11
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Device Summary
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.
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
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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