TETRAFILCON A
K-Number: K990606 · 1999-03-15
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Device Summary
Frequently Asked Questions
What is the TETRAFILCON A?
TETRAFILCON A is a medical device that received FDA 510(k) clearance on 1999-03-15. The listed applicant is CooperVision, Inc.. The 510(k) number is K990606.
When did TETRAFILCON A receive FDA 510(k) clearance?
TETRAFILCON A received FDA 510(k) clearance on 1999-03-15, under 510(k) number K990606.
Who is the listed applicant for TETRAFILCON A?
The FDA 510(k) record lists CooperVision, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for TETRAFILCON A?
The FDA product code for TETRAFILCON A 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 CooperVision, 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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