FDA 510(k)

PHILIPS ULTRASOUND P800 IMAGING SYSTEM

K-Number: K935923 · 1994-12-08

Decision Date1994-12-08

Product CodeIYN

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PHILIPS ULTRASOUND P800 IMAGING SYSTEM 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 1994-12-08 under 510(k) number K935923. 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 PHILIPS ULTRASOUND P800 IMAGING SYSTEM?

PHILIPS ULTRASOUND P800 IMAGING SYSTEM is a medical device that received FDA 510(k) clearance on 1994-12-08. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K935923.

When did PHILIPS ULTRASOUND P800 IMAGING SYSTEM receive FDA 510(k) clearance?

PHILIPS ULTRASOUND P800 IMAGING SYSTEM received FDA 510(k) clearance on 1994-12-08, under 510(k) number K935923.

Who is the listed applicant for PHILIPS ULTRASOUND P800 IMAGING SYSTEM?

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 PHILIPS ULTRASOUND P800 IMAGING SYSTEM?

The FDA product code for PHILIPS ULTRASOUND P800 IMAGING SYSTEM is IYN.

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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.