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FDA 510(k)

ANGIOSCANE SPECTRUM ANALYZER

K-Number: K834501 · 1984-05-23

ApplicantUnigon Industries, Inc.
Decision Date1984-05-23
Product Code
DecisionSubstantially Equivalent

Device Summary

ANGIOSCANE SPECTRUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Unigon Industries, Inc.. It received FDA 510(k) clearance on 1984-05-23 under 510(k) number K834501. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANGIOSCANE SPECTRUM ANALYZER?

ANGIOSCANE SPECTRUM ANALYZER is a medical device that received FDA 510(k) clearance on 1984-05-23. The listed applicant is Unigon Industries, Inc.. The 510(k) number is K834501.

When did ANGIOSCANE SPECTRUM ANALYZER receive FDA 510(k) clearance?

ANGIOSCANE SPECTRUM ANALYZER received FDA 510(k) clearance on 1984-05-23, under 510(k) number K834501.

Who is the listed applicant for ANGIOSCANE SPECTRUM ANALYZER?

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

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.

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Other records listing Unigon Industries, 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.

K834525ANGIOSCAN FLO MAD SPECTRUM ANALYZERK812184ANGIOSCAN SPECTRUM ANALYZER

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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