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FDA 510(k)

AV Viewer

K-Number: K250181 · 2025-07-15

ApplicantPhilips Medical Systems Nederland B.V.
Decision Date2025-07-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AV Viewer is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2025-07-15 under 510(k) number K250181. 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 AV Viewer?

AV Viewer is a medical device that received FDA 510(k) clearance on 2025-07-15. The listed applicant is Philips Medical Systems Nederland B.V.. The 510(k) number is K250181.

When did AV Viewer receive FDA 510(k) clearance?

AV Viewer received FDA 510(k) clearance on 2025-07-15, under 510(k) number K250181.

Who is the listed applicant for AV Viewer?

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

What is the FDA product code for AV Viewer?

The FDA product code for AV Viewer 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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