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FDA 510(k)

MANIFOLD, FOR DOUBLE SUPPLY

K-Number: K790154 · 1979-03-07

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

Device Summary

MANIFOLD, FOR DOUBLE SUPPLY 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 K790154. 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, FOR DOUBLE SUPPLY?

MANIFOLD, FOR DOUBLE SUPPLY 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 K790154.

When did MANIFOLD, FOR DOUBLE SUPPLY receive FDA 510(k) clearance?

MANIFOLD, FOR DOUBLE SUPPLY received FDA 510(k) clearance on 1979-03-07, under 510(k) number K790154.

Who is the listed applicant for MANIFOLD, FOR DOUBLE SUPPLY?

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, FOR DOUBLE SUPPLY?

The FDA product code for MANIFOLD, FOR DOUBLE SUPPLY 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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