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FDA 510(k)

BACTERIAL AND VIRAL FILTER

K-Number: K895233 · 1989-11-15

Decision Date1989-11-15
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BACTERIAL AND VIRAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is F.L.W. Plastics, Inc.. It received FDA 510(k) clearance on 1989-11-15 under 510(k) number K895233. 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 BACTERIAL AND VIRAL FILTER?

BACTERIAL AND VIRAL FILTER is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is F.L.W. Plastics, Inc.. The 510(k) number is K895233.

When did BACTERIAL AND VIRAL FILTER receive FDA 510(k) clearance?

BACTERIAL AND VIRAL FILTER received FDA 510(k) clearance on 1989-11-15, under 510(k) number K895233.

Who is the listed applicant for BACTERIAL AND VIRAL FILTER?

The FDA 510(k) record lists F.L.W. Plastics, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACTERIAL AND VIRAL FILTER?

The FDA product code for BACTERIAL AND VIRAL 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 F.L.W. Plastics, Inc. 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.

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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