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FDA 510(k)

CONTACT LENS CLEANSER

K-Number: K780823 · 1978-06-30

ApplicantKetchum Laboratories, Inc.
Decision Date1978-06-30
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

CONTACT LENS CLEANSER is the device name listed in this FDA 510(k) record. The listed applicant is Ketchum Laboratories, Inc.. It received FDA 510(k) clearance on 1978-06-30 under 510(k) number K780823. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTACT LENS CLEANSER?

CONTACT LENS CLEANSER is a medical device that received FDA 510(k) clearance on 1978-06-30. The listed applicant is Ketchum Laboratories, Inc.. The 510(k) number is K780823.

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

CONTACT LENS CLEANSER received FDA 510(k) clearance on 1978-06-30, under 510(k) number K780823.

Who is the listed applicant for CONTACT LENS CLEANSER?

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

What is the FDA product code for CONTACT LENS CLEANSER?

The FDA product code for CONTACT LENS CLEANSER 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

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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