510(k) K923172

ANAESTHESIA RECORD KEEPER by Datex Division Instrumentarium Corp. — Product Code BSZ

K923172 is an FDA 510(k) premarket notification submitted by Datex Division Instrumentarium Corp. for the device "ANAESTHESIA RECORD KEEPER". The FDA issued a decision of Substantially Equivalent on August 9, 1994. The device falls under product code BSZ (Gas-Machine, Anesthesia), a Class II device regulated under 21 CFR 868.5160. Datex Division Instrumentarium Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 9, 1994
Date Received
June 29, 1992
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Gas-Machine, Anesthesia
Device Class
Class II
Regulation Number
868.5160
Review Panel
AN
Submission Type