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FDA 510(k)

SERVO VENTILATOR 900E

K-Number: K884520 · 1989-01-17

ApplicantSiemens-Elema Ventilation Systems
Decision Date1989-01-17
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO VENTILATOR 900E is the device name listed in this FDA 510(k) record. The listed applicant is Siemens-Elema Ventilation Systems. It received FDA 510(k) clearance on 1989-01-17 under 510(k) number K884520. 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 VENTILATOR 900E?

SERVO VENTILATOR 900E is a medical device that received FDA 510(k) clearance on 1989-01-17. The listed applicant is Siemens-Elema Ventilation Systems. The 510(k) number is K884520.

When did SERVO VENTILATOR 900E receive FDA 510(k) clearance?

SERVO VENTILATOR 900E received FDA 510(k) clearance on 1989-01-17, under 510(k) number K884520.

Who is the listed applicant for SERVO VENTILATOR 900E?

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

What is the FDA product code for SERVO VENTILATOR 900E?

The FDA product code for SERVO VENTILATOR 900E is CBK.

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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.

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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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