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FDA 510(k)

LOBOB UNIVERSAL CONTACT LENS CLEANER

K-Number: K990044 · 1999-02-11

Decision Date1999-02-11
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LOBOB UNIVERSAL CONTACT LENS CLEANER is the device name listed in this FDA 510(k) record. The listed applicant is Lobob Laboratories, Inc.. It received FDA 510(k) clearance on 1999-02-11 under 510(k) number K990044. The device is classified under product code LPN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOBOB UNIVERSAL CONTACT LENS CLEANER?

LOBOB UNIVERSAL CONTACT LENS CLEANER is a medical device that received FDA 510(k) clearance on 1999-02-11. The listed applicant is Lobob Laboratories, Inc.. The 510(k) number is K990044.

When did LOBOB UNIVERSAL CONTACT LENS CLEANER receive FDA 510(k) clearance?

LOBOB UNIVERSAL CONTACT LENS CLEANER received FDA 510(k) clearance on 1999-02-11, under 510(k) number K990044.

Who is the listed applicant for LOBOB UNIVERSAL CONTACT LENS CLEANER?

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

What is the FDA product code for LOBOB UNIVERSAL CONTACT LENS CLEANER?

The FDA product code for LOBOB UNIVERSAL CONTACT LENS CLEANER is LPN.

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 Lobob Laboratories, 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: LPN)

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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