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FDA 510(k)

PHILIPS HARMONY RELEASE 1

K-Number: K022788 · 2002-10-25

ApplicantPhilips Medical Systems North America Co.
Decision Date2002-10-25
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS HARMONY RELEASE 1 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems North America Co.. It received FDA 510(k) clearance on 2002-10-25 under 510(k) number K022788. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PHILIPS HARMONY RELEASE 1?

PHILIPS HARMONY RELEASE 1 is a medical device that received FDA 510(k) clearance on 2002-10-25. The listed applicant is Philips Medical Systems North America Co.. The 510(k) number is K022788.

When did PHILIPS HARMONY RELEASE 1 receive FDA 510(k) clearance?

PHILIPS HARMONY RELEASE 1 received FDA 510(k) clearance on 2002-10-25, under 510(k) number K022788.

Who is the listed applicant for PHILIPS HARMONY RELEASE 1?

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

What is the FDA product code for PHILIPS HARMONY RELEASE 1?

The FDA product code for PHILIPS HARMONY RELEASE 1 is LLZ.

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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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