MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT— 510(k) K863756

Name: FDA 510(k) clearance K863756
Creator: U.S. Food and Drug Administration
Published: 1986-11-13

Substantially Equivalent

Nova-Ventrx

FDA 510(k) clearance K863756 for MODIFIED CRITERION VENTILATOR BREATHING CIRCUIT, Substantially Equivalent on 1986-11-13. Applicant: Nova-Ventrx. Device class: 1.

Clearance details

Applicant: Nova-Ventrx
Product code: Code BZO
Device class: Class 1
Regulation: 21 CFR 868.5975
Advisory panel: Anesthesiology
Date received: 1986-09-25
Decision date: 1986-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Wheeling, IL, 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 Nova-Ventrx

view all

K952267 — CRITERION, CRITERION I.V., MODIFIED1997-12-02
K954480 — CONDENSATE COLLECTION KIT1995-12-29
K893760 — CRITERION I.V. VENTILATOR BREATHING CIRCUIT #10041989-08-10
K881207 — RES-Q 1, 2, 3, 4 AND 51988-08-15
K870382 — DRV DISP RESUSCIT 3000/BAG ADAPT 3010 & 30111987-03-06

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