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FDA 510(k)

ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS

K-Number: K023350 · 2002-11-06

Decision Date2002-11-06
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS is the device name listed in this FDA 510(k) record. The listed applicant is Respironics California, Inc.. It received FDA 510(k) clearance on 2002-11-06 under 510(k) number K023350. 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 ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS?

ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS is a medical device that received FDA 510(k) clearance on 2002-11-06. The listed applicant is Respironics California, Inc.. The 510(k) number is K023350.

When did ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS receive FDA 510(k) clearance?

ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS received FDA 510(k) clearance on 2002-11-06, under 510(k) number K023350.

Who is the listed applicant for ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS?

The FDA 510(k) record lists Respironics California, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS?

The FDA product code for ESPRIT VENTILATOR WITH RESPIRATORY MECHANICS 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 Respironics California, 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 11 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

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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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