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FDA 510(k)

POLARIS DIAL-A-DATE CONTACT LENS CASE

K-Number: K120904 · 2012-11-26

Decision Date2012-11-26
Product CodeLRX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

POLARIS DIAL-A-DATE CONTACT LENS CASE is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Design & Manufacture Corp.. It received FDA 510(k) clearance on 2012-11-26 under 510(k) number K120904. 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 DIAL-A-DATE CONTACT LENS CASE?

POLARIS DIAL-A-DATE CONTACT LENS CASE is a medical device that received FDA 510(k) clearance on 2012-11-26. The listed applicant is Reliance Design & Manufacture Corp.. The 510(k) number is K120904.

When did POLARIS DIAL-A-DATE CONTACT LENS CASE receive FDA 510(k) clearance?

POLARIS DIAL-A-DATE CONTACT LENS CASE received FDA 510(k) clearance on 2012-11-26, under 510(k) number K120904.

Who is the listed applicant for POLARIS DIAL-A-DATE CONTACT LENS CASE?

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

What is the FDA product code for POLARIS DIAL-A-DATE CONTACT LENS CASE?

The FDA product code for POLARIS DIAL-A-DATE 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

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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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