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FDA 510(k)

MP-070-M RADIOAEROSOL KIT

K-Number: K862795 · 1986-08-01

ApplicantMedipart Jerry Alexander
Decision Date1986-08-01
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MP-070-M RADIOAEROSOL KIT is the device name listed in this FDA 510(k) record. The listed applicant is Medipart Jerry Alexander. It received FDA 510(k) clearance on 1986-08-01 under 510(k) number K862795. 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 MP-070-M RADIOAEROSOL KIT?

MP-070-M RADIOAEROSOL KIT is a medical device that received FDA 510(k) clearance on 1986-08-01. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K862795.

When did MP-070-M RADIOAEROSOL KIT receive FDA 510(k) clearance?

MP-070-M RADIOAEROSOL KIT received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862795.

Who is the listed applicant for MP-070-M RADIOAEROSOL KIT?

The FDA 510(k) record lists Medipart Jerry Alexander as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MP-070-M RADIOAEROSOL KIT?

The FDA product code for MP-070-M RADIOAEROSOL KIT is IYT.

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Other records listing Medipart Jerry Alexander 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.

K896885DISPOSABLE RESPIRTORY KIT (MP-200)K896125MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133MK896475DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELDK896124MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133K896476DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELDK894138MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD

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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

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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