FDA 510(k)

PULSED DOPPLER OPTION, CONTINU-WAVE

K-Number: K842407 · 1985-02-13

Decision Date1985-02-13

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PULSED DOPPLER OPTION, CONTINU-WAVE is the device name listed in this FDA 510(k) record. The listed applicant is General Electric Co.. It received FDA 510(k) clearance on 1985-02-13 under 510(k) number K842407. The device is classified under product code IYN. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PULSED DOPPLER OPTION, CONTINU-WAVE?

PULSED DOPPLER OPTION, CONTINU-WAVE is a medical device that received FDA 510(k) clearance on 1985-02-13. The listed applicant is General Electric Co.. The 510(k) number is K842407.

When did PULSED DOPPLER OPTION, CONTINU-WAVE receive FDA 510(k) clearance?

PULSED DOPPLER OPTION, CONTINU-WAVE received FDA 510(k) clearance on 1985-02-13, under 510(k) number K842407.

Who is the listed applicant for PULSED DOPPLER OPTION, CONTINU-WAVE?

The FDA 510(k) record lists General Electric Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PULSED DOPPLER OPTION, CONTINU-WAVE?

The FDA product code for PULSED DOPPLER OPTION, CONTINU-WAVE is IYN.

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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.