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FDA 510(k)

CONFEES(R)+ CONTACT LENS HOLDER

K-Number: K897084 · 1990-02-28

Decision Date1990-02-28
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

CONFEES(R)+ CONTACT LENS HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Magnivision, Inc.. It received FDA 510(k) clearance on 1990-02-28 under 510(k) number K897084. 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 CONFEES(R)+ CONTACT LENS HOLDER?

CONFEES(R)+ CONTACT LENS HOLDER is a medical device that received FDA 510(k) clearance on 1990-02-28. The listed applicant is Magnivision, Inc.. The 510(k) number is K897084.

When did CONFEES(R)+ CONTACT LENS HOLDER receive FDA 510(k) clearance?

CONFEES(R)+ CONTACT LENS HOLDER received FDA 510(k) clearance on 1990-02-28, under 510(k) number K897084.

Who is the listed applicant for CONFEES(R)+ CONTACT LENS HOLDER?

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

What is the FDA product code for CONFEES(R)+ CONTACT LENS HOLDER?

The FDA product code for CONFEES(R)+ CONTACT LENS HOLDER 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 Magnivision, Inc. 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 8 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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