510(k) K093023

PTFE PEELABLE INTRODUCER by Great Batch Medical — Product Code DYB

K093023 is an FDA 510(k) premarket notification submitted by Great Batch Medical for the device "PTFE PEELABLE INTRODUCER". The FDA issued a decision of Substantially Equivalent on October 29, 2009. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Great Batch Medical has at least 9 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 29, 2009
Date Received
September 29, 2009
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Introducer, Catheter
Device Class
Class II
Regulation Number
870.1340
Review Panel
CV
Submission Type