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FDA 510(k)

PHILIPS SONO DIAGNOST 800

K-Number: K963706 · 1997-03-19

ApplicantHewlett-Packard Co.
Decision Date1997-03-19
Product CodeIYO
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS SONO DIAGNOST 800 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 1997-03-19 under 510(k) number K963706. The device is classified under product code IYO. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS SONO DIAGNOST 800?

PHILIPS SONO DIAGNOST 800 is a medical device that received FDA 510(k) clearance on 1997-03-19. The listed applicant is Hewlett-Packard Co.. The 510(k) number is K963706.

When did PHILIPS SONO DIAGNOST 800 receive FDA 510(k) clearance?

PHILIPS SONO DIAGNOST 800 received FDA 510(k) clearance on 1997-03-19, under 510(k) number K963706.

Who is the listed applicant for PHILIPS SONO DIAGNOST 800?

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 SONO DIAGNOST 800?

The FDA product code for PHILIPS SONO DIAGNOST 800 is IYO.

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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.

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