FDA 510(k)

DOPPLER IMAGING OPTION

K-Number: K840140 · 1984-08-23

Decision Date1984-08-23

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DOPPLER IMAGING OPTION is the device name listed in this FDA 510(k) record. The listed applicant is Hewlett-Packard Co.. It received FDA 510(k) clearance on 1984-08-23 under 510(k) number K840140. 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 DOPPLER IMAGING OPTION?

DOPPLER IMAGING OPTION is a medical device that received FDA 510(k) clearance on 1984-08-23. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K840140.

When did DOPPLER IMAGING OPTION receive FDA 510(k) clearance?

DOPPLER IMAGING OPTION received FDA 510(k) clearance on 1984-08-23, under 510(k) number K840140.

Who is the listed applicant for DOPPLER IMAGING OPTION?

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

What is the FDA product code for DOPPLER IMAGING OPTION?

The FDA product code for DOPPLER IMAGING OPTION 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.