FDA 510(k)

DOPPLER OPTION FOR PLATINUM

K-Number: K902691 · 1991-01-02

Decision Date1991-01-02

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

DOPPLER OPTION FOR PLATINUM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-01-02 under 510(k) number K902691. 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 OPTION FOR PLATINUM?

DOPPLER OPTION FOR PLATINUM is a medical device that received FDA 510(k) clearance on 1991-01-02. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K902691.

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

DOPPLER OPTION FOR PLATINUM received FDA 510(k) clearance on 1991-01-02, under 510(k) number K902691.

Who is the listed applicant for DOPPLER OPTION FOR PLATINUM?

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

What is the FDA product code for DOPPLER OPTION FOR PLATINUM?

The FDA product code for DOPPLER OPTION FOR PLATINUM is IYN.

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Other records listing Philips Medical Systems, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.