510(k) K831261

SCI MED TUBING CONNECTORS by Scimed Life Systems, Inc. — Product Code DTL

K831261 is an FDA 510(k) premarket notification submitted by Scimed Life Systems, Inc. for the device "SCI MED TUBING CONNECTORS". The FDA issued a decision of Substantially Equivalent on Jun 3, 1983. The device falls under product code DTL (Adaptor, Stopcock, Manifold, Fitting, Cardiopulmonary Bypass), a Class II device regulated under 21 CFR 870.4290. Scimed Life Systems, Inc. has 108 other 510(k) clearances on record.

Clearance details

Decision
SESE (Substantially Equivalent)
Decision Date
Jun 3, 1983
Date Received
Apr 18, 1983
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
510(k) Exempt

Source: FDA 510(k) database entry for K831261. Report a data issue: hello@regdatalab.com.