PAFLUFOCON C AND E DAILY CONTACT LENS
K-Number: K002845 · 2000-12-08
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Device Summary
Frequently Asked Questions
What is the PAFLUFOCON C AND E DAILY CONTACT LENS?
PAFLUFOCON C AND E DAILY CONTACT LENS is a medical device that received FDA 510(k) clearance on 2000-12-08. The listed applicant is Paragon Vision Sciences. The 510(k) number is K002845.
When did PAFLUFOCON C AND E DAILY CONTACT LENS receive FDA 510(k) clearance?
PAFLUFOCON C AND E DAILY CONTACT LENS received FDA 510(k) clearance on 2000-12-08, under 510(k) number K002845.
Who is the listed applicant for PAFLUFOCON C AND E DAILY CONTACT LENS?
The FDA 510(k) record lists Paragon Vision Sciences as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PAFLUFOCON C AND E DAILY CONTACT LENS?
The FDA product code for PAFLUFOCON C AND E DAILY CONTACT LENS is HQD.
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 Paragon Vision Sciences 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: HQD)
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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