Philips VSC-MEDlib
K-Number: K242001 · 2025-04-04
Decision Date2025-04-04
Product CodeBZQ
Advisory CommitteeAN
DecisionSubstantially Equivalent
Device Summary
Philips VSC-MEDlib is a medical device manufactured by Philips Medical Systems Nederland B.V.. It received FDA 510(k) clearance on 2025-04-04 under approval number K242001. The device is classified under product code BZQ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Philips VSC-MEDlib?
Philips VSC-MEDlib is a medical device that received FDA 510(k) clearance on 2025-04-04. It is manufactured by Philips Medical Systems Nederland B.V.. The 510(k) number is K242001.
When was Philips VSC-MEDlib approved by the FDA?
Philips VSC-MEDlib received FDA 510(k) clearance on 2025-04-04, under approval number K242001.
What company makes Philips VSC-MEDlib?
Philips VSC-MEDlib is manufactured by Philips Medical Systems Nederland B.V..
What is the FDA product code for Philips VSC-MEDlib?
The FDA product code for Philips VSC-MEDlib is BZQ.
Other Devices by Philips Medical Systems Nederland B.V.
Related Devices (Code: BZQ)
K152911EarlySense Insight SytemEarlysense, Ltd.
K151940Thora-3Di, Model T-01Pneumacare Limited
K173976Masimo Acoustic Respiration Sensors, infant and neonateMasimo Corporation
K180079Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor Packs (different #), Hill-Rom Vitals Monitoring System powered by EarlySense: Sensor ActivationHill-Rom, Inc.
K171836EarlySense Bed Sensing UnitEarlysense, Ltd.
K190775The RHEA Vital Sign Vigilance SystemShenzhen Fiber Medical Technology Co. , Ltd.
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.