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FDA 510(k)

LENZ CLENZER

K-Number: K881739 · 1988-10-07

ApplicantLens Care, Inc.
Decision Date1988-10-07
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LENZ CLENZER is the device name listed in this FDA 510(k) record. The listed applicant is Lens Care, Inc.. It received FDA 510(k) clearance on 1988-10-07 under 510(k) number K881739. The device is classified under product code LYL. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LENZ CLENZER?

LENZ CLENZER is a medical device that received FDA 510(k) clearance on 1988-10-07. The listed applicant is Lens Care, Inc.. The 510(k) number is K881739.

When did LENZ CLENZER receive FDA 510(k) clearance?

LENZ CLENZER received FDA 510(k) clearance on 1988-10-07, under 510(k) number K881739.

Who is the listed applicant for LENZ CLENZER?

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

What is the FDA product code for LENZ CLENZER?

The FDA product code for LENZ CLENZER is LYL.

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Related Devices (Code: LYL)

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.

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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.

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