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FDA 510(k)

OPTI-FREE CONTACT LENS CASE

K-Number: K931620 · 1993-06-28

Decision Date1993-06-28
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTI-FREE CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Alcon Laboratories. It received FDA 510(k) clearance on 1993-06-28 under 510(k) number K931620. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OPTI-FREE CONTACT LENS CASE?

OPTI-FREE CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1993-06-28. The listed applicant is Alcon Laboratories. The 510(k) number is K931620.

When did OPTI-FREE CONTACT LENS CASE receive FDA 510(k) clearance?

OPTI-FREE CONTACT LENS CASE received FDA 510(k) clearance on 1993-06-28, under 510(k) number K931620.

Who is the listed applicant for OPTI-FREE CONTACT LENS CASE?

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 CONTACT LENS CASE?

The FDA product code for OPTI-FREE CONTACT LENS CASE is LRX.

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: LRX)

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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