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FDA 510(k)

LENSKEEPER LENS CARRYING CASE

K-Number: K843342 · 1984-11-19

ApplicantAllergan Pharmaceuticals, Inc.
Decision Date1984-11-19
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

LENSKEEPER LENS CARRYING CASE is the device name listed in this FDA 510(k) record. The listed applicant is Allergan Pharmaceuticals, Inc.. It received FDA 510(k) clearance on 1984-11-19 under 510(k) number K843342. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LENSKEEPER LENS CARRYING CASE?

LENSKEEPER LENS CARRYING CASE is a medical device that received FDA 510(k) clearance on 1984-11-19. The listed applicant is Allergan Pharmaceuticals, Inc.. The 510(k) number is K843342.

When did LENSKEEPER LENS CARRYING CASE receive FDA 510(k) clearance?

LENSKEEPER LENS CARRYING CASE received FDA 510(k) clearance on 1984-11-19, under 510(k) number K843342.

Who is the listed applicant for LENSKEEPER LENS CARRYING CASE?

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

What is the FDA product code for LENSKEEPER LENS CARRYING CASE?

The FDA product code for LENSKEEPER LENS CARRYING CASE 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

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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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