CLEVELAND TUBING, INC. VENTILATOR HOSES— 510(k) K932119

Name: FDA 510(k) clearance K932119
Creator: U.S. Food and Drug Administration
Published: 1993-06-23

Substantially Equivalent

Cleveland Tubing, Inc.

FDA 510(k) clearance K932119 for CLEVELAND TUBING, INC. VENTILATOR HOSES, Substantially Equivalent on 1993-06-23. Applicant: Cleveland Tubing, Inc.. Device class: 1.

Clearance details

Applicant: Cleveland Tubing, Inc.
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1993-05-03
Decision date: 1993-06-23
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Cleveland, TN, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BZO

view all

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 Cleveland Tubing, Inc.

view all

K945314 — CLEVELAND TUBING, INC. EXPANDABLE/COLLAPSIBLEMEDICAL TUBING1994-11-18
K940889 — CONNECTORS AND AIRWAY EXTENSIONS1994-11-10
K940890 — CORRUGATED TUBING1994-11-10

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