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FDA 510(k)

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD

K-Number: K894138 · 1989-09-26

ApplicantMedipart Jerry Alexander
Decision Date1989-09-26
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD 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 1989-09-26 under 510(k) number K894138. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD?

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD is a medical device that received FDA 510(k) clearance on 1989-09-26. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K894138.

When did MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD receive FDA 510(k) clearance?

MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD received FDA 510(k) clearance on 1989-09-26, under 510(k) number K894138.

Who is the listed applicant for MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD?

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 AEROSOL SYSTEM MP-070-PTD?

The FDA product code for MEDIPART DISPOSABLE AEROSOL SYSTEM MP-070-PTD is CAF.

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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-0133MK896124MEDIPART DISPOSABLE XENON-133 REBREATHING MP-0133K896476DISP. RADIOAEROSOL KIT (MP-400-M) TO FIT SHIELDK896475DISP. RADIOAEROSOL KIT (MP-400) TO FIT LEAD SHIELDK893532RESUBMITTED RADIOAEROSOL CONT. SYSTEM MP-963

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Related Devices (Code: CAF)

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.

K254171Mesh Nebulizer (UN204); Mesh Nebulizer (UN205); Mesh Nebulizer (UN209); Mesh Nebulizer (UN210)Shenzhen Mericonn Technology Co., Ltd.K260270FindAir ONE for pMDI (FAO-MDI-V12-GRE-001)FindAir Sp. z o.o.K251572eRapid with eTrack SystemPari Respiratory Equipment, Inc.K251659Mesh Nebulizer (H6)Qingdao Future Medical Technology Co., Ltd.K244035Portable mesh nebulizer (JM821)Shenzhen Jermei Medical Device Technology Co., Ltd.K243468Compressor Nebulizer (NB-1100); Compressor Nebulizer (NB-1101); Compressor Nebulizer (NB-1102); Compressor Nebulizer (NB-1103)Joytech Healthcare Co. , 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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