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FDA 510(k)

TRANSPARENT ANESTHESIA FILTER

K-Number: K944189 · 1994-10-28

ApplicantAnetec, Inc.
Decision Date1994-10-28
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TRANSPARENT ANESTHESIA FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Anetec, Inc.. It received FDA 510(k) clearance on 1994-10-28 under 510(k) number K944189. 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 TRANSPARENT ANESTHESIA FILTER?

TRANSPARENT ANESTHESIA FILTER is a medical device that received FDA 510(k) clearance on 1994-10-28. The listed applicant is Anetec, Inc.. The 510(k) number is K944189.

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

TRANSPARENT ANESTHESIA FILTER received FDA 510(k) clearance on 1994-10-28, under 510(k) number K944189.

Who is the listed applicant for TRANSPARENT ANESTHESIA FILTER?

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

What is the FDA product code for TRANSPARENT ANESTHESIA FILTER?

The FDA product code for TRANSPARENT ANESTHESIA FILTER is CAH.

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Other records listing Anetec, Inc. 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.

K891479DISPOSABLE THERMOPLASTIC ANESTH BREATHING CIRCUITS

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Official Source

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