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FDA 510(k)

ZEFON BATERIAL/VIRAL FILTER

K-Number: K911651 · 1991-05-30

Decision Date1991-05-30
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ZEFON BATERIAL/VIRAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Bill Olson Corp.. It received FDA 510(k) clearance on 1991-05-30 under 510(k) number K911651. 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 ZEFON BATERIAL/VIRAL FILTER?

ZEFON BATERIAL/VIRAL FILTER is a medical device that received FDA 510(k) clearance on 1991-05-30. The listed applicant is Bill Olson Corp.. The 510(k) number is K911651.

When did ZEFON BATERIAL/VIRAL FILTER receive FDA 510(k) clearance?

ZEFON BATERIAL/VIRAL FILTER received FDA 510(k) clearance on 1991-05-30, under 510(k) number K911651.

Who is the listed applicant for ZEFON BATERIAL/VIRAL FILTER?

The FDA 510(k) record lists Bill Olson Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ZEFON BATERIAL/VIRAL FILTER?

The FDA product code for ZEFON BATERIAL/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 Bill Olson Corp. 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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