510(k) K053019

ACUITY STEERABLE STYLET ACCESSORY by Guidant Corporation — Product Code DRB

K053019 is an FDA 510(k) premarket notification submitted by Guidant Corporation for the device "ACUITY STEERABLE STYLET ACCESSORY". The FDA issued a decision of Substantially Equivalent on March 3, 2006. The device falls under product code DRB (Stylet, Catheter), a Class II device regulated under 21 CFR 870.1380. Guidant Corporation has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 3, 2006
Date Received
October 26, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Stylet, Catheter
Device Class
Class II
Regulation Number
870.1380
Review Panel
CV
Submission Type