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FDA 510(k)

ANESTHESIA WORKSTATION

K-Number: K901474 · 1990-04-10

ApplicantSiemens Life Support Systems
Decision Date1990-04-10
Product CodeBRY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA WORKSTATION is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Life Support Systems. It received FDA 510(k) clearance on 1990-04-10 under 510(k) number K901474. The device is classified under product code BRY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANESTHESIA WORKSTATION?

ANESTHESIA WORKSTATION is a medical device that received FDA 510(k) clearance on 1990-04-10. The listed applicant is Siemens Life Support Systems. The 510(k) number is K901474.

When did ANESTHESIA WORKSTATION receive FDA 510(k) clearance?

ANESTHESIA WORKSTATION received FDA 510(k) clearance on 1990-04-10, under 510(k) number K901474.

Who is the listed applicant for ANESTHESIA WORKSTATION?

The FDA 510(k) record lists Siemens Life Support Systems as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ANESTHESIA WORKSTATION?

The FDA product code for ANESTHESIA WORKSTATION is BRY.

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.

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Other records listing Siemens Life Support Systems 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.

K902859SERVO VENTILATOR 300K903991PCM ANESTHESIAK893786SERVO ANESTHESIA CIRCLE 985K890932CAV 3.0C SOFTWARE PROGRAMK890921DATA EXCHANGE SYSTEM, MODEL 24

Related Devices (Code: BRY)

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.

K921710MOVIT DEVICEJohn J. Navar, M.D.K912346MEDIKEEPERMedikeeper, Inc.K871564ANESTHASSISTAnestech, Inc.K821307ANESTHECACHEMed-Life, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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