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FDA 510(k)

PRE VUE

K-Number: K830573 · 1983-03-29

ApplicantTaut, Inc.
Decision Date1983-03-29
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PRE VUE is the device name listed in this FDA 510(k) record. The listed applicant is Taut, Inc.. It received FDA 510(k) clearance on 1983-03-29 under 510(k) number K830573. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRE VUE?

PRE VUE is a medical device that received FDA 510(k) clearance on 1983-03-29. The listed applicant is Taut, Inc.. The 510(k) number is K830573.

When did PRE VUE receive FDA 510(k) clearance?

PRE VUE received FDA 510(k) clearance on 1983-03-29, under 510(k) number K830573.

Who is the listed applicant for PRE VUE?

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

What is the FDA product code for PRE VUE?

The FDA product code for PRE VUE is FOZ.

Other records listing Taut, 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.

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Related Devices (Code: FOZ)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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