510(k) K081045

DESTINATION RENAL GUIDING SHEATH by Terumo Medical Corp. — Product Code DYB

K081045 is an FDA 510(k) premarket notification submitted by Terumo Medical Corp. for the device "DESTINATION RENAL GUIDING SHEATH". The FDA issued a decision of Substantially Equivalent on May 28, 2008. The device falls under product code DYB (Introducer, Catheter), a Class II device regulated under 21 CFR 870.1340. Terumo Medical Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 28, 2008
Date Received
April 14, 2008
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