METHAFILCON A
K-Number: K002625 · 2000-09-13
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Device Summary
Frequently Asked Questions
What is the METHAFILCON A?
METHAFILCON A is a medical device that received FDA 510(k) clearance on 2000-09-13. The listed applicant is CooperVision, Inc.. The 510(k) number is K002625.
When did METHAFILCON A receive FDA 510(k) clearance?
METHAFILCON A received FDA 510(k) clearance on 2000-09-13, under 510(k) number K002625.
Who is the listed applicant for METHAFILCON 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 METHAFILCON A?
The FDA product code for METHAFILCON 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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