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FDA 510(k)

CORRUGATED FLEXIBLE POLYETHYLENE

K-Number: K790886 · 1979-05-17

ApplicantAirlife, Inc.
Decision Date1979-05-17
Product Code
DecisionSubstantially Equivalent

Device Summary

CORRUGATED FLEXIBLE POLYETHYLENE is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-05-17 under 510(k) number K790886. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CORRUGATED FLEXIBLE POLYETHYLENE?

CORRUGATED FLEXIBLE POLYETHYLENE is a medical device that received FDA 510(k) clearance on 1979-05-17. The listed applicant is Airlife, Inc.. The 510(k) number is K790886.

When did CORRUGATED FLEXIBLE POLYETHYLENE receive FDA 510(k) clearance?

CORRUGATED FLEXIBLE POLYETHYLENE received FDA 510(k) clearance on 1979-05-17, under 510(k) number K790886.

Who is the listed applicant for CORRUGATED FLEXIBLE POLYETHYLENE?

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

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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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