510(k) K890606

OHMEDA 5330 AGENT MONITOR by Ohmeda Medical — Product Code CBQ

K890606 is an FDA 510(k) premarket notification submitted by Ohmeda Medical for the device "OHMEDA 5330 AGENT MONITOR". The FDA issued a decision of Substantially Equivalent on April 20, 1989. The device falls under product code CBQ (Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)), a Class II device regulated under 21 CFR 868.1500. Ohmeda Medical has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 20, 1989
Date Received
February 6, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Gas, Enflurane, Gaseous-Phase (Anesthetic Concentration)
Device Class
Class II
Regulation Number
868.1500
Review Panel
AN
Submission Type