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FDA 510(k)

MODEL 600 VASCULAR DUPLEX IMAGER

K-Number: K863589 · 1987-06-24

ApplicantMultigon Industries, Inc.
Decision Date1987-06-24
Product CodeDXK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 600 VASCULAR DUPLEX IMAGER 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 1987-06-24 under 510(k) number K863589. The device is classified under product code DXK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 600 VASCULAR DUPLEX IMAGER?

MODEL 600 VASCULAR DUPLEX IMAGER is a medical device that received FDA 510(k) clearance on 1987-06-24. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K863589.

When did MODEL 600 VASCULAR DUPLEX IMAGER receive FDA 510(k) clearance?

MODEL 600 VASCULAR DUPLEX IMAGER received FDA 510(k) clearance on 1987-06-24, under 510(k) number K863589.

Who is the listed applicant for MODEL 600 VASCULAR DUPLEX IMAGER?

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 600 VASCULAR DUPLEX IMAGER?

The FDA product code for MODEL 600 VASCULAR DUPLEX IMAGER is DXK.

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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.

K052067DOPPLER GUIDED PROCTOSCOPE, MODEL 500HK051739POCKET TRANSCRANIAL AND VASCULAR DOPPLER SPECTRUM ANALYZER, MODEL 500P; PW DOPPLER ULTRAOUND PROBE, MODEL 2MPB.K912044MODEL 700 LAPAROSCOPIC ELECTRONIC INSUFFLATORK881263MODEL 500A VASCULAR SPECTRUM ANALYZER W/DOPPLERK882755MODEL 500V VASCULAR SPECTRUM ANALYZERK860435MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER

View all 8 devices →

Related Devices (Code: DXK)

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.

K181042Ultra ICE Plus – PI 9 MHz Peripheral Imaging CatheterBoston Scientific CorporationK160173Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter(eDFU), Ultra ICE Plus 9 MHz IntraCardiac Echo Catheter (Paper DFU)Boston Scientific CorporationK031148IN-VISION IMAGING SYSTEMJomed, Inc.K9348879750 ATHENA ETHERNET OPTIONS & W Medico Teknik A/SK913209ACCESSORY TO GENESIS III (GCFM)Biosound, Inc.K911384CATHSCANNER(R) VISIONS(TM) 3.5F 54700/5.0F 54600Endosonics Corp.

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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