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FDA 510(k)

CIRCUITS, BREATHING W/CONNECTORS, ADAPT

K-Number: K801875 · 1980-08-14

ApplicantAirlife, Inc.
Decision Date1980-08-14
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CIRCUITS, BREATHING W/CONNECTORS, ADAPT is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1980-08-14 under 510(k) number K801875. The device is classified under product code CAF. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CIRCUITS, BREATHING W/CONNECTORS, ADAPT?

CIRCUITS, BREATHING W/CONNECTORS, ADAPT is a medical device that received FDA 510(k) clearance on 1980-08-14. The listed applicant is Airlife, Inc.. The 510(k) number is K801875.

When did CIRCUITS, BREATHING W/CONNECTORS, ADAPT receive FDA 510(k) clearance?

CIRCUITS, BREATHING W/CONNECTORS, ADAPT received FDA 510(k) clearance on 1980-08-14, under 510(k) number K801875.

Who is the listed applicant for CIRCUITS, BREATHING W/CONNECTORS, ADAPT?

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

What is the FDA product code for CIRCUITS, BREATHING W/CONNECTORS, ADAPT?

The FDA product code for CIRCUITS, BREATHING W/CONNECTORS, ADAPT is CAF.

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Other records listing Airlife, Inc. 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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