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FDA 510(k)

HARD CONTACT LENS CASE

K-Number: K831973 · 1983-10-19

ApplicantMoonbeam International, Inc.
Decision Date1983-10-19
Product CodeHPX
DecisionSubstantially Equivalent

Device Summary

HARD CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Moonbeam International, Inc.. It received FDA 510(k) clearance on 1983-10-19 under 510(k) number K831973. The device is classified under product code HPX. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HARD CONTACT LENS CASE?

HARD CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 1983-10-19. The listed applicant is Moonbeam International, Inc.. The 510(k) number is K831973.

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

HARD CONTACT LENS CASE received FDA 510(k) clearance on 1983-10-19, under 510(k) number K831973.

Who is the listed applicant for HARD CONTACT LENS CASE?

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

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

The FDA product code for HARD CONTACT 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Moonbeam International, 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.

K840115SWISS OPTICAL PRODUCTS-CONTACT CASE

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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