Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133

K-Number: K896124 · 1990-01-22

ApplicantMedipart Jerry Alexander
Decision Date1990-01-22
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133 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 1990-01-22 under 510(k) number K896124. 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 MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133?

MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133 is a medical device that received FDA 510(k) clearance on 1990-01-22. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K896124.

When did MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133 receive FDA 510(k) clearance?

MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133 received FDA 510(k) clearance on 1990-01-22, under 510(k) number K896124.

Who is the listed applicant for MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133?

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 MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133?

The FDA product code for MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133 is IYT.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 SHIELDK896476DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELDK894138MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTDK893532RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963

View all 49 devices →

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.

↑