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FDA 510(k)

RCI VIRAL/BACTERIAL FILTER

K-Number: K892230 · 1989-08-28

ApplicantRespiratory Care, Inc.
Decision Date1989-08-28
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RCI VIRAL/BACTERIAL FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Respiratory Care, Inc.. It received FDA 510(k) clearance on 1989-08-28 under 510(k) number K892230. 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 RCI VIRAL/BACTERIAL FILTER?

RCI VIRAL/BACTERIAL FILTER is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Respiratory Care, Inc.. The 510(k) number is K892230.

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

RCI VIRAL/BACTERIAL FILTER received FDA 510(k) clearance on 1989-08-28, under 510(k) number K892230.

Who is the listed applicant for RCI VIRAL/BACTERIAL FILTER?

The FDA 510(k) record lists Respiratory Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RCI VIRAL/BACTERIAL FILTER?

The FDA product code for RCI VIRAL/BACTERIAL FILTER is CAH.

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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.

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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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