INTELLISAVE AX700 ANESTHESIA SYSTEM
K-Number: K122063 · 2013-08-02
Advertisement
Device Summary
Frequently Asked Questions
What is the INTELLISAVE AX700 ANESTHESIA SYSTEM?
INTELLISAVE AX700 ANESTHESIA SYSTEM is a medical device that received FDA 510(k) clearance on 2013-08-02. The listed applicant is Philips Anesthesia Care. The 510(k) number is K122063.
When did INTELLISAVE AX700 ANESTHESIA SYSTEM receive FDA 510(k) clearance?
INTELLISAVE AX700 ANESTHESIA SYSTEM received FDA 510(k) clearance on 2013-08-02, under 510(k) number K122063.
Who is the listed applicant for INTELLISAVE AX700 ANESTHESIA SYSTEM?
The FDA 510(k) record lists Philips Anesthesia Care as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTELLISAVE AX700 ANESTHESIA SYSTEM?
The FDA product code for INTELLISAVE AX700 ANESTHESIA SYSTEM is BSZ.
Related Clinical Trials
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: BSZ)
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.
Advertisement