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FDA 510(k)

CAV 3.0C SOFTWARE PROGRAM

K-Number: K890932 · 1989-06-12

ApplicantSiemens Life Support Systems
Decision Date1989-06-12
Product CodeBZK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAV 3.0C SOFTWARE PROGRAM 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 1989-06-12 under 510(k) number K890932. The device is classified under product code BZK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAV 3.0C SOFTWARE PROGRAM?

CAV 3.0C SOFTWARE PROGRAM is a medical device that received FDA 510(k) clearance on 1989-06-12. The listed applicant is Siemens Life Support Systems. The 510(k) number is K890932.

When did CAV 3.0C SOFTWARE PROGRAM receive FDA 510(k) clearance?

CAV 3.0C SOFTWARE PROGRAM received FDA 510(k) clearance on 1989-06-12, under 510(k) number K890932.

Who is the listed applicant for CAV 3.0C SOFTWARE PROGRAM?

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 CAV 3.0C SOFTWARE PROGRAM?

The FDA product code for CAV 3.0C SOFTWARE PROGRAM is BZK.

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 ANESTHESIAK901474ANESTHESIA WORKSTATIONK893786SERVO ANESTHESIA CIRCLE 985K890921DATA EXCHANGE SYSTEM, MODEL 24

Related Devices (Code: BZK)

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.

K260226ElintMAX Respiratory Monitor (ElintMAX Monitor A1)Amptron Medical, Inc.K192584BEACON Caresystem Model 00002144Mermaid Care A/SK192595ExSpiron 2XiRespiratory MotionK180788Gas Module 3Shenzhen Mindray Bio-Medical Electronics Co., Ltd.K173181ExSpiron 1XiRespiratory Motion, Inc.K162131ExSpiron 1XiRespiratory Motion, Inc.

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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