Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E

K-Number: K022132 · 2002-09-19

Decision Date2002-09-19
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E is the device name listed in this FDA 510(k) record. The listed applicant is Siemens Medical Solutions USA, Inc.. It received FDA 510(k) clearance on 2002-09-19 under 510(k) number K022132. 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 SYSTEM, MODEL 64 87 800 E407E?

SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E is a medical device that received FDA 510(k) clearance on 2002-09-19. The listed applicant is Siemens Medical Solutions USA, Inc.. The 510(k) number is K022132.

When did SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E receive FDA 510(k) clearance?

SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E received FDA 510(k) clearance on 2002-09-19, under 510(k) number K022132.

Who is the listed applicant for SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E?

The FDA 510(k) record lists Siemens Medical Solutions USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E?

The FDA product code for SERVO VENTILATOR SYSTEM, MODEL 64 87 800 E407E 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.

Other records listing Siemens Medical Solutions USA, Inc. 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.

View all 732 devices →

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.

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.

↑