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FDA 510(k)

VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840

K-Number: K063650 · 2007-02-15

Decision Date2007-02-15
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 2007-02-15 under 510(k) number K063650. 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 VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840?

VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 is a medical device that received FDA 510(k) clearance on 2007-02-15. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K063650.

When did VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 receive FDA 510(k) clearance?

VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 received FDA 510(k) clearance on 2007-02-15, under 510(k) number K063650.

Who is the listed applicant for VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840?

The FDA 510(k) record lists Puritan Bennett Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840?

The FDA product code for VENTILATOR WITH RESPIRATORY MECHANICS, MODEL 840 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 Puritan Bennett Corp. 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 110 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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