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FDA 510(k)

ANESTHESIA BACTERIA FILTER

K-Number: K801804 · 1980-08-13

ApplicantOmnicon Medical Corp.
Decision Date1980-08-13
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ANESTHESIA BACTERIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Omnicon Medical Corp.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801804. 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 ANESTHESIA BACTERIA FILTER?

ANESTHESIA BACTERIA FILTER is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Omnicon Medical Corp.. The 510(k) number is K801804.

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

ANESTHESIA BACTERIA FILTER received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801804.

Who is the listed applicant for ANESTHESIA BACTERIA FILTER?

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

What is the FDA product code for ANESTHESIA BACTERIA FILTER?

The FDA product code for ANESTHESIA BACTERIA FILTER is CAH.

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Other records listing Omnicon Medical 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.

K823872EMERGENCY TRACHEOSTOMY KITK820577ANESTHESIA BACTERIA FILTERK820576MAINFLOW BACTERIA FILTERK801803MAINFLOW BACTERIA FILTERK772060PROTECT IV GARDK770136DISPOSABLE BACTERIA FILTER

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Related Devices (Code: CAH)

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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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