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FDA 510(k)

XENON GAS BREATHING CIRCUIT

K-Number: K952223 · 1995-08-11

ApplicantIntertech Resources, Inc.
Decision Date1995-08-11
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

XENON GAS BREATHING CIRCUIT is the device name listed in this FDA 510(k) record. The listed applicant is Intertech Resources, Inc.. It received FDA 510(k) clearance on 1995-08-11 under 510(k) number K952223. 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 XENON GAS BREATHING CIRCUIT?

XENON GAS BREATHING CIRCUIT is a medical device that received FDA 510(k) clearance on 1995-08-11. The listed applicant is Intertech Resources, Inc.. The 510(k) number is K952223.

When did XENON GAS BREATHING CIRCUIT receive FDA 510(k) clearance?

XENON GAS BREATHING CIRCUIT received FDA 510(k) clearance on 1995-08-11, under 510(k) number K952223.

Who is the listed applicant for XENON GAS BREATHING CIRCUIT?

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

What is the FDA product code for XENON GAS BREATHING CIRCUIT?

The FDA product code for XENON GAS BREATHING CIRCUIT is IYT.

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Other records listing Intertech Resources, 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.

K9613181ST RESPONSE DISPOSABLE MANOMETERK955008HEAT & MOISTURE EXCHANGERK953580HEAT MOISTURE EXCHANGERK952169SAFE RESPONSE MOUTH-TO-MASK RESUSCITATOR, PEDIATRICK952062PFT FILTERK952214SIMS INTERTECH HYPERINFLATION BAG SYSTEM

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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.K914747XENON CIRCUITGibeck, Inc.K913416TETLEY PATIENT ADMINISTRATION SETTetley Medical , Ltd.K912626BOLUS XENON CIRCUITVital Signs, Inc.

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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