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FDA 510(k)

OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP

K-Number: K984573 · 1999-09-16

Decision Date1999-09-16
Product CodeLPN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1999-09-16 under 510(k) number K984573. 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 OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP?

OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP is a medical device that received FDA 510(k) clearance on 1999-09-16. The listed applicant is Alcon Laboratories. The 510(k) number is K984573.

When did OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP receive FDA 510(k) clearance?

OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP received FDA 510(k) clearance on 1999-09-16, under 510(k) number K984573.

Who is the listed applicant for OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP?

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

What is the FDA product code for OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP?

The FDA product code for OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP 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 Alcon Laboratories 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.

View all 47 devices →

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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