FDA 510(k)

PROCLEAR DAILY WEAR CONTACT LENS

K-Number: K952152 · 1995-07-27

Decision Date1995-07-27

Product CodeLPL

Advisory CommitteeOP

DecisionSubstantially Equivalent

Device Summary

PROCLEAR DAILY WEAR CONTACT LENS is the device name listed in this FDA 510(k) record. The listed applicant is Biocompatibles , Ltd.. It received FDA 510(k) clearance on 1995-07-27 under 510(k) number K952152. The device is classified under product code LPL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PROCLEAR DAILY WEAR CONTACT LENS?

PROCLEAR DAILY WEAR CONTACT LENS is a medical device that received FDA 510(k) clearance on 1995-07-27. The listed applicant is Biocompatibles , Ltd.. The 510(k) number is K952152.

When did PROCLEAR DAILY WEAR CONTACT LENS receive FDA 510(k) clearance?

PROCLEAR DAILY WEAR CONTACT LENS received FDA 510(k) clearance on 1995-07-27, under 510(k) number K952152.

Who is the listed applicant for PROCLEAR DAILY WEAR CONTACT LENS?

The FDA 510(k) record lists Biocompatibles , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PROCLEAR DAILY WEAR CONTACT LENS?

The FDA product code for PROCLEAR DAILY WEAR CONTACT LENS is LPL.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.