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FDA 510(k)

JET VENTILATOR/JETTING DEVICE

K-Number: K921926 · 1992-10-13

ApplicantAnesthesia Assoc., Inc.
Decision Date1992-10-13
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

JET VENTILATOR/JETTING DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Anesthesia Assoc., Inc.. It received FDA 510(k) clearance on 1992-10-13 under 510(k) number K921926. The device is classified under product code BTL. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JET VENTILATOR/JETTING DEVICE?

JET VENTILATOR/JETTING DEVICE is a medical device that received FDA 510(k) clearance on 1992-10-13. The listed applicant is Anesthesia Assoc., Inc.. The 510(k) number is K921926.

When did JET VENTILATOR/JETTING DEVICE receive FDA 510(k) clearance?

JET VENTILATOR/JETTING DEVICE received FDA 510(k) clearance on 1992-10-13, under 510(k) number K921926.

Who is the listed applicant for JET VENTILATOR/JETTING DEVICE?

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

What is the FDA product code for JET VENTILATOR/JETTING DEVICE?

The FDA product code for JET VENTILATOR/JETTING DEVICE is BTL.

Related Clinical Trials

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Other records listing Anesthesia Assoc., 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.

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Related Devices (Code: BTL)

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.

K242769VentStar Resus heated (N) (MP17030); VentStar Autobreath heated (N) (MP17031)Draegerwerk AG & CO KgaaK221634Oxymag - Transport and Emergency VentilatorMagnamed Tecnologia Medica S/AK202219VORTRAN GO2VENT with PEEP ValveVortran Medical Technology 1, Inc.K193191MEDUMAT Easy CPR, MEDUMAT Easy CPR with bagWeinmann Emergency Medical Technology GmbH + Co. KGK182956Puffin Lite Infant Resuscitation SystemInternational BiomedicalK173373SafeT T-Piece ResuscitatorVentlab, LLC

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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