Y & ELBOW W/WO PORTS— 510(k) K791856

Substantially Equivalent

Airlife, Inc.

FDA 510(k) clearance K791856 for Y & ELBOW W/WO PORTS, Substantially Equivalent on 1979-09-26. Applicant: Airlife, Inc.. Device class: 1.

Clearance details

Applicant: Airlife, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1979-09-19
Decision date: 1979-09-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZO

K953784 — UNICOR, INC. CORRUGATED TUBING1995-09-19
K953785 — UNICOR, INC. VENTILATOR HOSES1995-09-18
K952010 — PRIMA VENTILATOR HOSES1995-05-22
K952011 — PRIMA BREATHING BAGS1995-05-22
K952012 — PRIMA CUSTOM ANESTESIA CIRCUIT1995-05-22

More clearances from Airlife, Inc.

K834570 — VOLUME VENTILATOR CIRCUIT W/WATER TRAP1984-03-05
K834573 — AQUA 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

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