Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

POLARIS CONTACT LENS CASE

K-Number: K093377 · 2010-04-27

Decision Date2010-04-27
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

POLARIS CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Design & Manufacturing Corp.. It received FDA 510(k) clearance on 2010-04-27 under 510(k) number K093377. The device is classified under product code LRX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POLARIS CONTACT LENS CASE?

POLARIS CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2010-04-27. The listed applicant is Reliance Design & Manufacturing Corp.. The 510(k) number is K093377.

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

POLARIS CONTACT LENS CASE received FDA 510(k) clearance on 2010-04-27, under 510(k) number K093377.

Who is the listed applicant for POLARIS CONTACT LENS CASE?

The FDA 510(k) record lists Reliance Design & Manufacturing Corp. as the applicant. This does not by itself establish the device manufacturer.

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

The FDA product code for POLARIS CONTACT LENS CASE is LRX.

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.

Related Devices (Code: LRX)

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.

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.

↑