510(k) K021282

LV-1 HEMOSTASIS VALVE, MODEL #6789 by Guidant Corp. — Product Code DTL

K021282 is an FDA 510(k) premarket notification submitted by Guidant Corp. for the device "LV-1 HEMOSTASIS VALVE, MODEL #6789". The FDA issued a decision of Substantially Equivalent on May 2, 2002. The device falls under product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4290. Guidant Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 2, 2002
Date Received
April 18, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass
Device Class
Class II
Regulation Number
870.4290
Review Panel
CV
Submission Type