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FDA 510(k)

AQUALUX LENS CASE

K-Number: K862811 · 1986-09-03

ApplicantSafeway Products, Inc.
Decision Date1986-09-03
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

AQUALUX LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Safeway Products, Inc.. It received FDA 510(k) clearance on 1986-09-03 under 510(k) number K862811. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AQUALUX LENS CASE?

AQUALUX LENS CASE is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Safeway Products, Inc.. The 510(k) number is K862811.

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

AQUALUX LENS CASE received FDA 510(k) clearance on 1986-09-03, under 510(k) number K862811.

Who is the listed applicant for AQUALUX LENS CASE?

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

What is the FDA product code for AQUALUX LENS CASE?

The FDA product code for AQUALUX LENS CASE is HPX.

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.

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Other records listing Safeway Products, 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.

K891508PATIENT EXAMINATION GLOVES (LATEX)K822828SOFT LENS THERMAL DISINFECTING UNIT, A-C

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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