UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV
K-Number: K071526 · 2008-12-10
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Device Summary
Frequently Asked Questions
What is the UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV?
UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV is a medical device that received FDA 510(k) clearance on 2008-12-10. The listed applicant is Impact Instrumentation, Inc.. The 510(k) number is K071526.
When did UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV receive FDA 510(k) clearance?
UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV received FDA 510(k) clearance on 2008-12-10, under 510(k) number K071526.
Who is the listed applicant for UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV?
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 731 SERIES VENTILATORS, MODEL 731, 731EMV?
The FDA product code for UNI-VENT 731 SERIES VENTILATORS, MODEL 731, 731EMV 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.
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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