510(k) K892387

MODIFIED GELMAN ARTERIAL FILTER by Gelman Sciences, Inc. — Product Code DTM

K892387 is an FDA 510(k) premarket notification submitted by Gelman Sciences, Inc. for the device "MODIFIED GELMAN ARTERIAL FILTER". The FDA issued a decision of Substantially Equivalent on June 22, 1989. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Gelman Sciences, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 22, 1989
Date Received
April 14, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Filter, Blood, Cardiopulmonary Bypass, Arterial Line
Device Class
Class II
Regulation Number
870.4260
Review Panel
CV
Submission Type