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FDA 510(k)

CLENSATRON AUTOMATIC CONTACT LENS CLEANER

K-Number: K884414 · 1988-12-29

Decision Date1988-12-29
Product CodeLYL
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CLENSATRON AUTOMATIC CONTACT LENS CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Questech Intl., Inc.. It received FDA 510(k) clearance on 1988-12-29 under 510(k) number K884414. 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 CLENSATRON AUTOMATIC CONTACT LENS CLEANER?

CLENSATRON AUTOMATIC CONTACT LENS CLEANER is a medical device that received FDA 510(k) clearance on 1988-12-29. The listed applicant is Questech Intl., Inc.. The 510(k) number is K884414.

When did CLENSATRON AUTOMATIC CONTACT LENS CLEANER receive FDA 510(k) clearance?

CLENSATRON AUTOMATIC CONTACT LENS CLEANER received FDA 510(k) clearance on 1988-12-29, under 510(k) number K884414.

Who is the listed applicant for CLENSATRON AUTOMATIC CONTACT LENS CLEANER?

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

What is the FDA product code for CLENSATRON AUTOMATIC CONTACT LENS CLEANER?

The FDA product code for CLENSATRON AUTOMATIC CONTACT LENS CLEANER is LYL.

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 Questech Intl., 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: 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.

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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