Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

AV Viewer

K-Number: K250181 · 2025-07-15

Decision Date2025-07-15
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

AV Viewer is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2025-07-15 under approval 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. 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.

View all 77 devices →

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.