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FDA 510(k)

RAD VALVE

K-Number: K830404 · 1983-03-17

ApplicantKhi, Inc.
Decision Date1983-03-17
Product CodeBTL
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RAD VALVE is the device name listed in this FDA 510(k) record. The listed applicant is Khi, Inc.. It received FDA 510(k) clearance on 1983-03-17 under 510(k) number K830404. 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 RAD VALVE?

RAD VALVE is a medical device that received FDA 510(k) clearance on 1983-03-17. The listed applicant is Khi, Inc.. The 510(k) number is K830404.

When did RAD VALVE receive FDA 510(k) clearance?

RAD VALVE received FDA 510(k) clearance on 1983-03-17, under 510(k) number K830404.

Who is the listed applicant for RAD VALVE?

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

What is the FDA product code for RAD VALVE?

The FDA product code for RAD VALVE is BTL.

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.

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Other records listing Khi, 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.

K830399COUPLING/VALVEK811858KHI CPRAM BREATHING CIRCUITK800456EMERGIENCY RESUSCITATOR/INHALOR W/ASPIR.

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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