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FDA 510(k)

LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM

K-Number: K050856 · 2005-05-31

Decision Date2005-05-31
Product CodeHOY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ophthocare , Ltd.. It received FDA 510(k) clearance on 2005-05-31 under 510(k) number K050856. The device is classified under product code HOY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM?

LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-31. The listed applicant is Ophthocare , Ltd.. The 510(k) number is K050856.

When did LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM receive FDA 510(k) clearance?

LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM received FDA 510(k) clearance on 2005-05-31, under 510(k) number K050856.

Who is the listed applicant for LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM?

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

What is the FDA product code for LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM?

The FDA product code for LCG (LIQUIDE CRYSTAL GLASSES) SYSTEM is HOY.

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: HOY)

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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