510(k) K143463

IS4/DF4 Port Plug by Oscor, Inc. — Product Code DTD

K143463 is an FDA 510(k) premarket notification submitted by Oscor, Inc. for the device "IS4/DF4 Port Plug". The FDA issued a decision of Substantially Equivalent on March 19, 2015. The device falls under product code DTD (Pacemaker Lead Adaptor), a Class II device regulated under 21 CFR 870.3620. Oscor, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 19, 2015
Date Received
December 4, 2014
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Pacemaker Lead Adaptor
Device Class
Class II
Regulation Number
870.3620
Review Panel
CV
Submission Type