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FDA 510(k)

INTELLISAVE AX700 ANESTHESIA SYSTEM

K-Number: K122063 · 2013-08-02

Decision Date2013-08-02
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

INTELLISAVE AX700 ANESTHESIA SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Philips Anesthesia Care. It received FDA 510(k) clearance on 2013-08-02 under 510(k) number K122063. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

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