510(k) K893760

CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004 by Nova-Ventrx — Product Code BZO

K893760 is an FDA 510(k) premarket notification submitted by Nova-Ventrx for the device "CRITERION I.V. VENTILATOR BREATHING CIRCUIT #1004". The FDA issued a decision of Substantially Equivalent on August 10, 1989. The device falls under product code BZO (Set, Tubing And Support, Ventilator (W Harness)), a Class I device regulated under 21 CFR 868.5975. Nova-Ventrx has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 10, 1989
Date Received
May 19, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Set, Tubing And Support, Ventilator (W Harness)
Device Class
Class I
Regulation Number
868.5975
Review Panel
AN
Submission Type