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FDA 510(k)

MP-1204 DISPOSABLE BACTERIA FILTER

K-Number: K862785 · 1986-08-01

ApplicantMedipart Jerry Alexander
Decision Date1986-08-01
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MP-1204 DISPOSABLE BACTERIA FILTER 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 K862785. 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 MP-1204 DISPOSABLE BACTERIA FILTER?

MP-1204 DISPOSABLE BACTERIA FILTER 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 K862785.

When did MP-1204 DISPOSABLE BACTERIA FILTER receive FDA 510(k) clearance?

MP-1204 DISPOSABLE BACTERIA FILTER received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862785.

Who is the listed applicant for MP-1204 DISPOSABLE BACTERIA FILTER?

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-1204 DISPOSABLE BACTERIA FILTER?

The FDA product code for MP-1204 DISPOSABLE BACTERIA FILTER is CAH.

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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: CAH)

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.

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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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