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FDA 510(k)

DOPPLER FLOW METER, LASER

K-Number: K827818 · 1982-08-20

ApplicantAtl Interspec Cardiology
Decision Date1982-08-20
Product Code
DecisionSubstantially Equivalent

Device Summary

DOPPLER FLOW METER, LASER is the device name listed in this FDA 510(k) record. The listed applicant is Atl Interspec Cardiology. It received FDA 510(k) clearance on 1982-08-20 under 510(k) number K827818. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DOPPLER FLOW METER, LASER?

DOPPLER FLOW METER, LASER is a medical device that received FDA 510(k) clearance on 1982-08-20. The listed applicant is Atl Interspec Cardiology. The 510(k) number is K827818.

When did DOPPLER FLOW METER, LASER receive FDA 510(k) clearance?

DOPPLER FLOW METER, LASER received FDA 510(k) clearance on 1982-08-20, under 510(k) number K827818.

Who is the listed applicant for DOPPLER FLOW METER, LASER?

The FDA 510(k) record lists Atl Interspec Cardiology as the applicant. This does not by itself establish the device manufacturer.

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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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