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FDA 510(k)

FACE TENT-VINYL

K-Number: K790884 · 1979-05-17

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

Device Summary

FACE TENT-VINYL 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 K790884. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FACE TENT-VINYL?

FACE TENT-VINYL 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 K790884.

When did FACE TENT-VINYL receive FDA 510(k) clearance?

FACE TENT-VINYL received FDA 510(k) clearance on 1979-05-17, under 510(k) number K790884.

Who is the listed applicant for FACE TENT-VINYL?

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

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.

K834573AQUA TRAPK834570VOLUME VENTILATOR CIRCUIT W/WATER TRAPK834077SINGLE USE NEBULIZER-ADJUST-AIR ENTRAINK833196VOLUME VENTILATOR CIRCUIT-NEBULIZERK833197TRACH SWIVE/CONNECTORK832725DUAL DIAL VENTURI STYLE MASK

View all 76 devices →

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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