IntelliVue Measurement Rack 6000 (867317)
K-Number: K253654 · 2026-03-30
Device Summary
Frequently Asked Questions
What is the IntelliVue Measurement Rack 6000 (867317)?
IntelliVue Measurement Rack 6000 (867317) is a medical device that received FDA 510(k) clearance on 2026-03-30. The listed applicant is Philips Medizin Systeme Böblingen GmbH. The 510(k) number is K253654.
When did IntelliVue Measurement Rack 6000 (867317) receive FDA 510(k) clearance?
IntelliVue Measurement Rack 6000 (867317) received FDA 510(k) clearance on 2026-03-30, under 510(k) number K253654.
Who is the listed applicant for IntelliVue Measurement Rack 6000 (867317)?
The FDA 510(k) record lists Philips Medizin Systeme Böblingen GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IntelliVue Measurement Rack 6000 (867317)?
The FDA product code for IntelliVue Measurement Rack 6000 (867317) is MSX.
Other records listing Philips Medizin Systeme Böblingen GmbH as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: MSX)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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.