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FDA 510(k)

VINGMED DS100 DOPPLER FLOWMETER

K-Number: K843933 · 1985-02-13

ApplicantVingmed, Inc.
Decision Date1985-02-13
Product CodeJAF
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

VINGMED DS100 DOPPLER FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Vingmed, Inc.. It received FDA 510(k) clearance on 1985-02-13 under 510(k) number K843933. 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 VINGMED DS100 DOPPLER FLOWMETER?

VINGMED DS100 DOPPLER FLOWMETER is a medical device that received FDA 510(k) clearance on 1985-02-13. The listed applicant is Vingmed, Inc.. The 510(k) number is K843933.

When did VINGMED DS100 DOPPLER FLOWMETER receive FDA 510(k) clearance?

VINGMED DS100 DOPPLER FLOWMETER received FDA 510(k) clearance on 1985-02-13, under 510(k) number K843933.

Who is the listed applicant for VINGMED DS100 DOPPLER FLOWMETER?

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

What is the FDA product code for VINGMED DS100 DOPPLER FLOWMETER?

The FDA product code for VINGMED DS100 DOPPLER FLOWMETER is JAF.

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 Vingmed, 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.

K855229CFM-10 VINGMED COLOR FLOW MAPPING SYSTEM

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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