510(k) K981231

CO2 by Abbott Mfg., Inc. — Product Code KHS

K981231 is an FDA 510(k) premarket notification submitted by Abbott Mfg., Inc. for the device "CO2". The FDA issued a decision of Substantially Equivalent on May 12, 1998. The device falls under product code KHS (Enzymatic, Carbon-Dioxide), a Class II device regulated under 21 CFR 862.1160. Abbott Mfg., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 12, 1998
Date Received
April 3, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Enzymatic, Carbon-Dioxide
Device Class
Class II
Regulation Number
862.1160
Review Panel
CH
Submission Type