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FDA 510(k)

PHILIPS DIGITAL IMAGING OPTION RELEASE 1

K-Number: K023440 · 2002-10-30

ApplicantPhilips Medical Systems
Decision Date2002-10-30
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PHILIPS DIGITAL IMAGING OPTION RELEASE 1 is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems. It received FDA 510(k) clearance on 2002-10-30 under 510(k) number K023440. 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 DIGITAL IMAGING OPTION RELEASE 1?

PHILIPS DIGITAL IMAGING OPTION RELEASE 1 is a medical device that received FDA 510(k) clearance on 2002-10-30. The listed applicant is Philips Medical Systems. The 510(k) number is K023440.

When did PHILIPS DIGITAL IMAGING OPTION RELEASE 1 receive FDA 510(k) clearance?

PHILIPS DIGITAL IMAGING OPTION RELEASE 1 received FDA 510(k) clearance on 2002-10-30, under 510(k) number K023440.

Who is the listed applicant for PHILIPS DIGITAL IMAGING OPTION RELEASE 1?

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

What is the FDA product code for PHILIPS DIGITAL IMAGING OPTION RELEASE 1?

The FDA product code for PHILIPS DIGITAL IMAGING OPTION RELEASE 1 is LLZ.

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Other records listing Philips Medical Systems as applicant

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Related Devices (Code: 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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