OPTI-FREE EXPRESS MULTI-ACTION CLEANING AND REWETTING DROP
K-Number: K984573 · 1999-09-16
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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