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FDA 510(k)

SERVO ANESTHESIA CIRCLE 985

K-Number: K893786 · 1989-09-22

ApplicantSiemens Life Support Systems
Decision Date1989-09-22
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO ANESTHESIA CIRCLE 985 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 1989-09-22 under 510(k) number K893786. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SERVO ANESTHESIA CIRCLE 985?

SERVO ANESTHESIA CIRCLE 985 is a medical device that received FDA 510(k) clearance on 1989-09-22. The listed applicant is Siemens Life Support Systems. The 510(k) number is K893786.

When did SERVO ANESTHESIA CIRCLE 985 receive FDA 510(k) clearance?

SERVO ANESTHESIA CIRCLE 985 received FDA 510(k) clearance on 1989-09-22, under 510(k) number K893786.

Who is the listed applicant for SERVO ANESTHESIA CIRCLE 985?

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 SERVO ANESTHESIA CIRCLE 985?

The FDA product code for SERVO ANESTHESIA CIRCLE 985 is CBK.

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 WORKSTATIONK890932CAV 3.0C SOFTWARE PROGRAMK890921DATA EXCHANGE SYSTEM, MODEL 24

Related Devices (Code: CBK)

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.

K253647Evita (V800); Evita (V600)Draegerwerk AG & CO KgaaK252663Inbentus VersatileIconic Solutions by Murcia, SLK251888VPAP Pediatric Face MaskHsiner Co., Ltd.K232365Vivo 45 LSOconnell Regulatory Consultants, Inc.K252173F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size A (ONIV117A); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size B (ONIV117B); F&P OptiNIV Hospital Vented Full Face Mask Compatible with Single-limb Circuits – Size C (ONIV117C); F&P OptiNIV ONIV117-F Hospital Vented Full Face Mask with optional Expiratory Filter Compatible with Single-limb Circuits - Size A (ONIV117A-F); F&P OptiNIV ONIV117-F Hospital Vented FullFisher & Paykel Healthcare, Ltd.K243767SV600, SV800 VentilatorShenzhen Mindray Bio-Medical Electronics Co., Ltd.

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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