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FDA 510(k)

OPTI-LENS CONTACT LENS CASE

K-Number: K920064 · 1992-03-04

Decision Date1992-03-04
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

OPTI-LENS CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Ryder Intl. Corp.. It received FDA 510(k) clearance on 1992-03-04 under 510(k) number K920064. 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-LENS CONTACT LENS CASE?

OPTI-LENS CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1992-03-04. The listed applicant is Ryder Intl. Corp.. The 510(k) number is K920064.

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

OPTI-LENS CONTACT LENS CASE received FDA 510(k) clearance on 1992-03-04, under 510(k) number K920064.

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

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

What is the FDA product code for OPTI-LENS CONTACT LENS CASE?

The FDA product code for OPTI-LENS 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 Ryder Intl. Corp. 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 10 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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