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FDA 510(k)

CONTACT LENS MATERL

K-Number: K811010 · 1981-12-09

ApplicantParagon Optical Co.
Decision Date1981-12-09
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

CONTACT LENS MATERL is the device name listed in this FDA 510(k) record. The listed applicant is Paragon Optical Co.. It received FDA 510(k) clearance on 1981-12-09 under 510(k) number K811010. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT LENS MATERL?

CONTACT LENS MATERL is a medical device that received FDA 510(k) clearance on 1981-12-09. The listed applicant is Paragon Optical Co.. The 510(k) number is K811010.

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

CONTACT LENS MATERL received FDA 510(k) clearance on 1981-12-09, under 510(k) number K811010.

Who is the listed applicant for CONTACT LENS MATERL?

The FDA 510(k) record lists Paragon Optical Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTACT LENS MATERL?

The FDA product code for CONTACT LENS MATERL is HPX.

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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

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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