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FDA 510(k)

UNIFILTER ANESTHESIA & RESPIRATORY FILT

K-Number: K841581 · 1984-04-30

ApplicantDupaco, Inc.
Decision Date1984-04-30
Product CodeCAH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

UNIFILTER ANESTHESIA & RESPIRATORY FILT is the device name listed in this FDA 510(k) record. The listed applicant is Dupaco, Inc.. It received FDA 510(k) clearance on 1984-04-30 under 510(k) number K841581. 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 UNIFILTER ANESTHESIA & RESPIRATORY FILT?

UNIFILTER ANESTHESIA & RESPIRATORY FILT is a medical device that received FDA 510(k) clearance on 1984-04-30. The listed applicant is Dupaco, Inc.. The 510(k) number is K841581.

When did UNIFILTER ANESTHESIA & RESPIRATORY FILT receive FDA 510(k) clearance?

UNIFILTER ANESTHESIA & RESPIRATORY FILT received FDA 510(k) clearance on 1984-04-30, under 510(k) number K841581.

Who is the listed applicant for UNIFILTER ANESTHESIA & RESPIRATORY FILT?

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

What is the FDA product code for UNIFILTER ANESTHESIA & RESPIRATORY FILT?

The FDA product code for UNIFILTER ANESTHESIA & RESPIRATORY FILT is CAH.

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Other records listing Dupaco, Inc. as applicant

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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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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