FDA 510(k)

5 MHZ DOPPLER OUTRIGGER

K-Number: K872817 · 1988-02-08

Decision Date1988-02-08

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

5 MHZ DOPPLER OUTRIGGER is the device name listed in this FDA 510(k) record. The listed applicant is Philips Ultrasound, Inc.. It received FDA 510(k) clearance on 1988-02-08 under 510(k) number K872817. 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 5 MHZ DOPPLER OUTRIGGER?

5 MHZ DOPPLER OUTRIGGER is a medical device that received FDA 510(k) clearance on 1988-02-08. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K872817.

When did 5 MHZ DOPPLER OUTRIGGER receive FDA 510(k) clearance?

5 MHZ DOPPLER OUTRIGGER received FDA 510(k) clearance on 1988-02-08, under 510(k) number K872817.

Who is the listed applicant for 5 MHZ DOPPLER OUTRIGGER?

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

What is the FDA product code for 5 MHZ DOPPLER OUTRIGGER?

The FDA product code for 5 MHZ DOPPLER OUTRIGGER 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.