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FDA 510(k)

ALTEX MODEL UST-3000E

K-Number: K924033 · 1992-11-05

ApplicantOptro-Mechanics (Usa) Corp.
Decision Date1992-11-05
Product CodeHQC
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

ALTEX MODEL UST-3000E is the device name listed in this FDA 510(k) record. The listed applicant is Optro-Mechanics (Usa) Corp.. It received FDA 510(k) clearance on 1992-11-05 under 510(k) number K924033. The device is classified under product code HQC. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALTEX MODEL UST-3000E?

ALTEX MODEL UST-3000E is a medical device that received FDA 510(k) clearance on 1992-11-05. The listed applicant is Optro-Mechanics (Usa) Corp.. The 510(k) number is K924033.

When did ALTEX MODEL UST-3000E receive FDA 510(k) clearance?

ALTEX MODEL UST-3000E received FDA 510(k) clearance on 1992-11-05, under 510(k) number K924033.

Who is the listed applicant for ALTEX MODEL UST-3000E?

The FDA 510(k) record lists Optro-Mechanics (Usa) Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALTEX MODEL UST-3000E?

The FDA product code for ALTEX MODEL UST-3000E is HQC.

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Related Devices (Code: HQC)

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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