OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS
K-Number: K972454 · 1997-08-08
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Device Summary
Frequently Asked Questions
What is the OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS?
OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS is a medical device that received FDA 510(k) clearance on 1997-08-08. The listed applicant is Bausch & Lomb, Inc.. The 510(k) number is K972454.
When did OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS receive FDA 510(k) clearance?
OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS received FDA 510(k) clearance on 1997-08-08, under 510(k) number K972454.
Who is the listed applicant for OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS?
The FDA 510(k) record lists Bausch & Lomb, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS?
The FDA product code for OXYCOR (BALAFILCON A) VISIBILITY TINTED CONTACT LENS 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 Bausch & Lomb, 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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