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FDA 510(k)

TWO-WAY ANESTHESIA FILTER

K-Number: K790896 · 1979-06-05

ApplicantPharmaseal Div., Baxter Healthcare Corp.
Decision Date1979-06-05
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TWO-WAY ANESTHESIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1979-06-05 under 510(k) number K790896. 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 TWO-WAY ANESTHESIA FILTER?

TWO-WAY ANESTHESIA FILTER is a medical device that received FDA 510(k) clearance on 1979-06-05. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. The 510(k) number is K790896.

When did TWO-WAY ANESTHESIA FILTER receive FDA 510(k) clearance?

TWO-WAY ANESTHESIA FILTER received FDA 510(k) clearance on 1979-06-05, under 510(k) number K790896.

Who is the listed applicant for TWO-WAY ANESTHESIA FILTER?

The FDA 510(k) record lists Pharmaseal Div., Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TWO-WAY ANESTHESIA FILTER?

The FDA product code for TWO-WAY ANESTHESIA FILTER is CAH.

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Other records listing Pharmaseal Div., Baxter Healthcare 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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