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FDA 510(k)

ALCON CONTACT LENS CASE

K-Number: K974281 · 1998-01-20

Decision Date1998-01-20
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALCON 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 1998-01-20 under 510(k) number K974281. 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 ALCON CONTACT LENS CASE?

ALCON CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1998-01-20. The listed applicant is Alcon Laboratories. The 510(k) number is K974281.

When did ALCON CONTACT LENS CASE receive FDA 510(k) clearance?

ALCON CONTACT LENS CASE received FDA 510(k) clearance on 1998-01-20, under 510(k) number K974281.

Who is the listed applicant for ALCON 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 ALCON CONTACT LENS CASE?

The FDA product code for ALCON 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

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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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