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FDA 510(k)

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H

K-Number: K052067 · 2005-08-29

ApplicantMultigon Industries, Inc.
Decision Date2005-08-29
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H 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 2005-08-29 under 510(k) number K052067. The device is classified under product code JAF. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOPPLER GUIDED PROCTOSCOPE, MODEL 500H?

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H is a medical device that received FDA 510(k) clearance on 2005-08-29. The listed applicant is Multigon Industries, Inc.. The 510(k) number is K052067.

When did DOPPLER GUIDED PROCTOSCOPE, MODEL 500H receive FDA 510(k) clearance?

DOPPLER GUIDED PROCTOSCOPE, MODEL 500H received FDA 510(k) clearance on 2005-08-29, under 510(k) number K052067.

Who is the listed applicant for DOPPLER GUIDED PROCTOSCOPE, MODEL 500H?

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 DOPPLER GUIDED PROCTOSCOPE, MODEL 500H?

The FDA product code for DOPPLER GUIDED PROCTOSCOPE, MODEL 500H is JAF.

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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.

K051739POCKET 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 ANALYZERK863589MODEL 600 VASCULAR DUPLEX IMAGERK860435MODEL 500A VASCULAR SPECTRUM ANALYZER W/CW DOPPLER

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Related Devices (Code: JAF)

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.

K242487Laminar P1 (LDH-HW-001)Laminar Digital Health, Inc.K110628SIMPLEABINewman MedicalK093393LIFEDOP MODEL 300ABISummit Doppler Systems, Inc.K090009THD SLIDE ONEThd SpaK081429THD SLIDEThd SpaK070815THDG.F. S.R.L.

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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