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FDA 510(k)

BACTERIA FILTER

K-Number: K890035 · 1989-05-05

Decision Date1989-05-05
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Hudson Oxygen Therapy Sales Co.. It received FDA 510(k) clearance on 1989-05-05 under 510(k) number K890035. 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 BACTERIA FILTER?

BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1989-05-05. The listed applicant is Hudson Oxygen Therapy Sales Co.. The 510(k) number is K890035.

When did BACTERIA FILTER receive FDA 510(k) clearance?

BACTERIA FILTER received FDA 510(k) clearance on 1989-05-05, under 510(k) number K890035.

Who is the listed applicant for BACTERIA FILTER?

The FDA 510(k) record lists Hudson Oxygen Therapy Sales Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BACTERIA FILTER?

The FDA product code for BACTERIA 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 Hudson Oxygen Therapy Sales Co. 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 33 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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