AQUA TRAP— 510(k) K834573

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K834573 for AQUA TRAP, Substantially Equivalent on 1984-03-05. Applicant: Airlife, Inc.. Device class: 1.

Clearance details

Applicant: Airlife, Inc.
Product code: Code BYH
Device class: Class 1
Regulation: 21 CFR 868.5995
Advisory panel: Anesthesiology
Date received: 1983-12-29
Decision date: 1984-03-05
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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More clearances from Airlife, Inc.

K834570 — VOLUME VENTILATOR CIRCUIT W/WATER TRAP1984-03-05
K834077 — SINGLE USE NEBULIZER-ADJUST-AIR ENTRAIN1983-12-12
K833196 — VOLUME VENTILATOR CIRCUIT-NEBULIZER1983-11-03
K833197 — TRACH SWIVE/CONNECTOR1983-10-28
K832725 — DUAL DIAL VENTURI STYLE MASK1983-09-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.