510(k) K981530

SPACELABS MEDICAL 90519 ANESTHESIA DELIVERY SYSTEM by Spacelabs Medical, Inc. — Product Code BSZ

K981530 is an FDA 510(k) premarket notification submitted by Spacelabs Medical, Inc. for the device "SPACELABS MEDICAL 90519 ANESTHESIA DELIVERY SYSTEM". The FDA issued a decision of Substantially Equivalent on November 20, 1998. The device falls under product code BSZ (Gas-Machine, Anesthesia), a Class II device regulated under 21 CFR 868.5160. Spacelabs Medical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 20, 1998
Date Received
April 29, 1998
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