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FDA 510(k)

MODEL 500V VASCULAR SPECTRUM ANALYZER

K-Number: K882755 · 1988-11-29

Decision Date1988-11-29
Product CodeIYN
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 500V VASCULAR SPECTRUM ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Multigon Industries, Inc.. It received FDA 510(k) clearance on 1988-11-29 under 510(k) number K882755. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 500V VASCULAR SPECTRUM ANALYZER?

MODEL 500V VASCULAR SPECTRUM ANALYZER is a medical device that received FDA 510(k) clearance on 1988-11-29. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K882755.

When did MODEL 500V VASCULAR SPECTRUM ANALYZER receive FDA 510(k) clearance?

MODEL 500V VASCULAR SPECTRUM ANALYZER received FDA 510(k) clearance on 1988-11-29, under 510(k) number K882755.

Who is the listed applicant for MODEL 500V VASCULAR SPECTRUM ANALYZER?

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

What is the FDA product code for MODEL 500V VASCULAR SPECTRUM ANALYZER?

The FDA product code for MODEL 500V VASCULAR SPECTRUM ANALYZER is IYN.

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 Multigon 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.

View all 8 devices →

Related Devices (Code: IYN)

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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