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FDA 510(k)

TEE ADAPTER

K-Number: K792364 · 1979-12-04

ApplicantAirlife, Inc.
Decision Date1979-12-04
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TEE ADAPTER is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-12-04 under 510(k) number K792364. 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 TEE ADAPTER?

TEE ADAPTER is a medical device that received FDA 510(k) clearance on 1979-12-04. The listed applicant is Airlife, Inc.. The 510(k) number is K792364.

When did TEE ADAPTER receive FDA 510(k) clearance?

TEE ADAPTER received FDA 510(k) clearance on 1979-12-04, under 510(k) number K792364.

Who is the listed applicant for TEE ADAPTER?

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 TEE ADAPTER?

The FDA product code for TEE ADAPTER is CAF.

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Related Devices (Code: CAF)

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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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