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FDA 510(k)

OREXAS POTENTEST

K-Number: K830158 · 1983-02-07

ApplicantOrexas Medical Corp.
Decision Date1983-02-07
Product CodeLIL
DecisionSubstantially Equivalent

Device Summary

OREXAS POTENTEST is the device name listed in this FDA 510(k) record. The listed applicant is Orexas Medical Corp.. It received FDA 510(k) clearance on 1983-02-07 under 510(k) number K830158. The device is classified under product code LIL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OREXAS POTENTEST?

OREXAS POTENTEST is a medical device that received FDA 510(k) clearance on 1983-02-07. The listed applicant is Orexas Medical Corp.. The 510(k) number is K830158.

When did OREXAS POTENTEST receive FDA 510(k) clearance?

OREXAS POTENTEST received FDA 510(k) clearance on 1983-02-07, under 510(k) number K830158.

Who is the listed applicant for OREXAS POTENTEST?

The FDA 510(k) record lists Orexas Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for OREXAS POTENTEST?

The FDA product code for OREXAS POTENTEST is LIL.

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Related Devices (Code: LIL)

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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