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FDA 510(k)

MANIFOLD, W/CORRUGATED TUBING

K-Number: K790153 · 1979-03-07

ApplicantAirlife, Inc.
Decision Date1979-03-07
Product CodeCAF
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MANIFOLD, W/CORRUGATED TUBING is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-03-07 under 510(k) number K790153. 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 MANIFOLD, W/CORRUGATED TUBING?

MANIFOLD, W/CORRUGATED TUBING is a medical device that received FDA 510(k) clearance on 1979-03-07. The listed applicant is Airlife, Inc.. The 510(k) number is K790153.

When did MANIFOLD, W/CORRUGATED TUBING receive FDA 510(k) clearance?

MANIFOLD, W/CORRUGATED TUBING received FDA 510(k) clearance on 1979-03-07, under 510(k) number K790153.

Who is the listed applicant for MANIFOLD, W/CORRUGATED TUBING?

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 MANIFOLD, W/CORRUGATED TUBING?

The FDA product code for MANIFOLD, W/CORRUGATED TUBING is 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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