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FDA 510(k)

OMNIFILTER MAIN FLOW BACTERIA FILTER

K-Number: K890362 · 1989-03-14

ApplicantPuritan Bennett Corp.
Decision Date1989-03-14
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

OMNIFILTER MAIN FLOW BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1989-03-14 under 510(k) number K890362. 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 OMNIFILTER MAIN FLOW BACTERIA FILTER?

OMNIFILTER MAIN FLOW BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1989-03-14. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K890362.

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

OMNIFILTER MAIN FLOW BACTERIA FILTER received FDA 510(k) clearance on 1989-03-14, under 510(k) number K890362.

Who is the listed applicant for OMNIFILTER MAIN FLOW BACTERIA FILTER?

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

What is the FDA product code for OMNIFILTER MAIN FLOW BACTERIA FILTER?

The FDA product code for OMNIFILTER MAIN FLOW BACTERIA FILTER is CAH.

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Other records listing Puritan Bennett Corp. as applicant

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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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