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FDA 510(k)

DISPOSABLE RESPIRTORY KIT (MP-200)

K-Number: K896885 · 1990-02-26

ApplicantMedipart Jerry Alexander
Decision Date1990-02-26
Product CodeIYT
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE RESPIRTORY KIT (MP-200) 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 1990-02-26 under 510(k) number K896885. 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 DISPOSABLE RESPIRTORY KIT (MP-200)?

DISPOSABLE RESPIRTORY KIT (MP-200) is a medical device that received FDA 510(k) clearance on 1990-02-26. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K896885.

When did DISPOSABLE RESPIRTORY KIT (MP-200) receive FDA 510(k) clearance?

DISPOSABLE RESPIRTORY KIT (MP-200) received FDA 510(k) clearance on 1990-02-26, under 510(k) number K896885.

Who is the listed applicant for DISPOSABLE RESPIRTORY KIT (MP-200)?

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 DISPOSABLE RESPIRTORY KIT (MP-200)?

The FDA product code for DISPOSABLE RESPIRTORY KIT (MP-200) 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.

K896125MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133MK896124MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133K896476DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELDK896475DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELDK894138MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTDK893532RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963

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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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