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FDA 510(k)

LENS, HARD CONTACT

K-Number: K760126 · 1976-07-20

ApplicantTru-Form Optics, Inc.
Decision Date1976-07-20
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

LENS, HARD CONTACT is the device name listed in this FDA 510(k) record. The listed applicant is Tru-Form Optics, Inc.. It received FDA 510(k) clearance on 1976-07-20 under 510(k) number K760126. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LENS, HARD CONTACT?

LENS, HARD CONTACT is a medical device that received FDA 510(k) clearance on 1976-07-20. The listed applicant is Tru-Form Optics, Inc.. The 510(k) number is K760126.

When did LENS, HARD CONTACT receive FDA 510(k) clearance?

LENS, HARD CONTACT received FDA 510(k) clearance on 1976-07-20, under 510(k) number K760126.

Who is the listed applicant for LENS, HARD CONTACT?

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

What is the FDA product code for LENS, HARD CONTACT?

The FDA product code for LENS, HARD CONTACT is HPX.

Related Clinical Trials

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Related Devices (Code: HPX)

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.

K955777PMMA CLASICRand Scientific Corp.K940106KERATOPLASTY SUTURING LENSVisionary Technologies of Miami, Inc.K913081MULTI-VIEW BIFOCALSCamp Contact LensesK897021MARTIN-HENSLEY SEGMENT LENSBruce W. Martin O.D. and Edward HensleyK895411OPTIKEM PMMA CONTACT LENSOptikem Polymers, Inc.K874591ILLUMINATING INFUSION CONTACT LENS FOR EYE SURGERYVitreo Dynamics, Co.

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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