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FDA 510(k)

MEDIPART BACTERIA FILTER MP-30X

K-Number: K844492 · 1984-12-04

ApplicantMedipart Jerry Alexander
Decision Date1984-12-04
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MEDIPART BACTERIA FILTER MP-30X 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 1984-12-04 under 510(k) number K844492. The device is classified under product code CAH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDIPART BACTERIA FILTER MP-30X?

MEDIPART BACTERIA FILTER MP-30X is a medical device that received FDA 510(k) clearance on 1984-12-04. The listed applicant is Medipart Jerry Alexander. The 510(k) number is K844492.

When did MEDIPART BACTERIA FILTER MP-30X receive FDA 510(k) clearance?

MEDIPART BACTERIA FILTER MP-30X received FDA 510(k) clearance on 1984-12-04, under 510(k) number K844492.

Who is the listed applicant for MEDIPART BACTERIA FILTER MP-30X?

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 BACTERIA FILTER MP-30X?

The FDA product code for MEDIPART BACTERIA FILTER MP-30X is CAH.

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Other records listing Medipart Jerry Alexander as applicant

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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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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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