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FDA 510(k)

MP-50T DISPOSABLE BREATHING CIRCUIT FILTER

K-Number: K862786 · 1986-08-01

Decision Date1986-08-01
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MP-50T DISPOSABLE BREATHING CIRCUIT 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 K862786. 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-50T DISPOSABLE BREATHING CIRCUIT FILTER?

MP-50T DISPOSABLE BREATHING CIRCUIT 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 K862786.

When did MP-50T DISPOSABLE BREATHING CIRCUIT FILTER receive FDA 510(k) clearance?

MP-50T DISPOSABLE BREATHING CIRCUIT FILTER received FDA 510(k) clearance on 1986-08-01, under 510(k) number K862786.

Who is the listed applicant for MP-50T DISPOSABLE BREATHING CIRCUIT 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-50T DISPOSABLE BREATHING CIRCUIT FILTER?

The FDA product code for MP-50T DISPOSABLE BREATHING CIRCUIT FILTER is CAH.

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.

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.

View all 49 devices →

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.

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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