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FDA 510(k)

AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE

K-Number: K850265 · 1985-04-05

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1985-04-05
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1985-04-05 under 510(k) number K850265. 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 AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE?

AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE is a medical device that received FDA 510(k) clearance on 1985-04-05. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K850265.

When did AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE receive FDA 510(k) clearance?

AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE received FDA 510(k) clearance on 1985-04-05, under 510(k) number K850265.

Who is the listed applicant for AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE?

The FDA product code for AMERICAN TWA WAY FILTER -BACTERIAL/VIRAL-RETENTIVE is CAH.

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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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