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FDA 510(k)

TETLEY PATIENT ADMINISTRATION SET

K-Number: K913416 · 1991-10-28

ApplicantTetley Medical , Ltd.
Decision Date1991-10-28
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

TETLEY PATIENT ADMINISTRATION SET is the device name listed in this FDA 510(k) record. The listed applicant is Tetley Medical , Ltd.. It received FDA 510(k) clearance on 1991-10-28 under 510(k) number K913416. 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 TETLEY PATIENT ADMINISTRATION SET?

TETLEY PATIENT ADMINISTRATION SET is a medical device that received FDA 510(k) clearance on 1991-10-28. The listed applicant is Tetley Medical , Ltd.. The 510(k) number is K913416.

When did TETLEY PATIENT ADMINISTRATION SET receive FDA 510(k) clearance?

TETLEY PATIENT ADMINISTRATION SET received FDA 510(k) clearance on 1991-10-28, under 510(k) number K913416.

Who is the listed applicant for TETLEY PATIENT ADMINISTRATION SET?

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

What is the FDA product code for TETLEY PATIENT ADMINISTRATION SET?

The FDA product code for TETLEY PATIENT ADMINISTRATION SET 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.K912626BOLUS XENON CIRCUITVital Signs, Inc.

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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