AV Viewer
K-Number: K250181 · 2025-07-15
Device Summary
Frequently Asked Questions
What is the AV Viewer?
AV Viewer is a medical device that received FDA 510(k) clearance on 2025-07-15. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K250181.
When was AV Viewer approved by the FDA?
AV Viewer received FDA 510(k) clearance on 2025-07-15, under approval number K250181.
What company makes AV Viewer?
AV Viewer is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for AV Viewer?
The FDA product code for AV Viewer is LLZ.
Other Devices by Philips Medical Systems Nederland B.V.
Related Devices (Code: LLZ)
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.