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FDA 510(k)

AVOXIMETER

K-Number: K932954 · 1993-12-27

Decision Date1993-12-27
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AVOXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is A-Vox Systems, Inc.. It received FDA 510(k) clearance on 1993-12-27 under 510(k) number K932954. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AVOXIMETER?

AVOXIMETER is a medical device that received FDA 510(k) clearance on 1993-12-27. The listed applicant is A-Vox Systems, Inc.. The 510(k) number is K932954.

When did AVOXIMETER receive FDA 510(k) clearance?

AVOXIMETER received FDA 510(k) clearance on 1993-12-27, under 510(k) number K932954.

Who is the listed applicant for AVOXIMETER?

The FDA 510(k) record lists A-Vox Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AVOXIMETER?

The FDA product code for AVOXIMETER is DQK.

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.

Other records listing A-Vox Systems, Inc. as applicant

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: DQK)

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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