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FDA 510(k)

UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR

K-Number: K111473 · 2012-02-16

Decision Date2012-02-16
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Impact Instrumentation, Inc.. It received FDA 510(k) clearance on 2012-02-16 under 510(k) number K111473. 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 UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR?

UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR is a medical device that received FDA 510(k) clearance on 2012-02-16. The listed applicant is Impact Instrumentation, Inc.. The 510(k) number is K111473.

When did UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR receive FDA 510(k) clearance?

UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR received FDA 510(k) clearance on 2012-02-16, under 510(k) number K111473.

Who is the listed applicant for UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR?

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

What is the FDA product code for UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR?

The FDA product code for UNI-VENT (R) MODEL 731 SERIES PORTABLE CRITICAL CARE VENTILATOR 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 Impact Instrumentation, 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 26 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.

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