510(k) K920594

SHILEY PERFUSION TUBING SETS by Shiley, Inc. — Product Code DTM

K920594 is an FDA 510(k) premarket notification submitted by Shiley, Inc. for the device "SHILEY PERFUSION TUBING SETS". The FDA issued a decision of Substantially Equivalent on March 18, 1993. The device falls under product code DTM (Filter, Blood, Cardiopulmonary Bypass, Arterial Line), a Class II device regulated under 21 CFR 870.4260. Shiley, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 18, 1993
Date Received
February 11, 1992
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