Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER

K-Number: K860435 · 1986-05-05

Decision Date1986-05-05
Product CodeDPT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER 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 1986-05-05 under 510(k) number K860435. The device is classified under product code DPT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER?

MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER is a medical device that received FDA 510(k) clearance on 1986-05-05. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K860435.

When did MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER receive FDA 510(k) clearance?

MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER received FDA 510(k) clearance on 1986-05-05, under 510(k) number K860435.

Who is the listed applicant for MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER?

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 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER?

The FDA product code for MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER is DPT.

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: DPT)

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

View on FDA Database →

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

↑