Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TUBING CORRUGATED

K-Number: K790147 · 1979-02-08

ApplicantAirlife, Inc.
Decision Date1979-02-08
Product CodeBYX
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

TUBING CORRUGATED is the device name listed in this FDA 510(k) record. The listed applicant is Airlife, Inc.. It received FDA 510(k) clearance on 1979-02-08 under 510(k) number K790147. The device is classified under product code BYX. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TUBING CORRUGATED?

TUBING CORRUGATED is a medical device that received FDA 510(k) clearance on 1979-02-08. The listed applicant is Airlife, Inc.. The 510(k) number is K790147.

When did TUBING CORRUGATED receive FDA 510(k) clearance?

TUBING CORRUGATED received FDA 510(k) clearance on 1979-02-08, under 510(k) number K790147.

Who is the listed applicant for TUBING CORRUGATED?

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 TUBING CORRUGATED?

The FDA product code for TUBING CORRUGATED is BYX.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Airlife, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 76 devices →

Related Devices (Code: BYX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.

↑