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FDA 510(k)

ILWAIT TIMER OCULOPRESSOR

K-Number: K112952 · 2012-05-10

ApplicantOryx Medical Pty, Ltd.
Decision Date2012-05-10
Product CodeLCC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ILWAIT TIMER OCULOPRESSOR is the device name listed in this FDA 510(k) record. The listed applicant is Oryx Medical Pty, Ltd.. It received FDA 510(k) clearance on 2012-05-10 under 510(k) number K112952. The device is classified under product code LCC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ILWAIT TIMER OCULOPRESSOR?

ILWAIT TIMER OCULOPRESSOR is a medical device that received FDA 510(k) clearance on 2012-05-10. The listed applicant is Oryx Medical Pty, Ltd.. The 510(k) number is K112952.

When did ILWAIT TIMER OCULOPRESSOR receive FDA 510(k) clearance?

ILWAIT TIMER OCULOPRESSOR received FDA 510(k) clearance on 2012-05-10, under 510(k) number K112952.

Who is the listed applicant for ILWAIT TIMER OCULOPRESSOR?

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

What is the FDA product code for ILWAIT TIMER OCULOPRESSOR?

The FDA product code for ILWAIT TIMER OCULOPRESSOR is LCC.

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Related Devices (Code: LCC)

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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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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