PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS
K-Number: K974408 · 1998-04-16
Advertisement
Device Summary
Frequently Asked Questions
What is the PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS?
PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS is a medical device that received FDA 510(k) clearance on 1998-04-16. The listed applicant is Biocompatibles Eyewear, Inc.. The 510(k) number is K974408.
When did PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS receive FDA 510(k) clearance?
PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS received FDA 510(k) clearance on 1998-04-16, under 510(k) number K974408.
Who is the listed applicant for PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS?
The FDA 510(k) record lists Biocompatibles Eyewear, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PROCLEAR (OMAFILCON A) DAILY WEAR CONTACT LENS?
The FDA product code for PROCLEAR (OMAFILCON A) DAILY WEAR 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 Biocompatibles Eyewear, 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.
Advertisement