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FDA 510(k)

DISPENSOR, XENON GAS

K-Number: K781933 · 1978-12-04

ApplicantDiagnostic Isotapes, Inc.
Decision Date1978-12-04
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DISPENSOR, XENON GAS is the device name listed in this FDA 510(k) record. The listed applicant is Diagnostic Isotapes, Inc.. It received FDA 510(k) clearance on 1978-12-04 under 510(k) number K781933. The device is classified under product code IYT. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPENSOR, XENON GAS?

DISPENSOR, XENON GAS is a medical device that received FDA 510(k) clearance on 1978-12-04. The listed applicant is Diagnostic Isotapes, Inc.. The 510(k) number is K781933.

When did DISPENSOR, XENON GAS receive FDA 510(k) clearance?

DISPENSOR, XENON GAS received FDA 510(k) clearance on 1978-12-04, under 510(k) number K781933.

Who is the listed applicant for DISPENSOR, XENON GAS?

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

What is the FDA product code for DISPENSOR, XENON GAS?

The FDA product code for DISPENSOR, XENON GAS is IYT.

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Related Devices (Code: IYT)

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.

K253942Pulmonex II Xenon System (132-503)Mirion Technologies (Capintec), Inc.K200916Patient Administration SetCyclomedica Australia Pty, Ltd.K953513XENON CIRCUITKing Systems Corp.K952223XENON GAS BREATHING CIRCUITIntertech Resources, Inc.K914747XENON CIRCUITGibeck, Inc.K913416TETLEY PATIENT ADMINISTRATION SETTetley Medical , Ltd.

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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