FDA 510(k) Applications Submitted by HANNAH FOLEY
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K140080 |
01/14/2014 |
ENVOY DISTAL ACCESS (DA) GUIDING CATHETER, 6F, 95CM & 105CM, STRAIGHT & XB, MPD & XB, MPC & XB |
Codman & Shurtleff, Inc. |
| K140307 |
02/07/2014 |
ENVOY GUIDING CATHETER |
Codman & Shurtleff, Inc. |
| K150319 |
02/09/2015 |
MICRUSFRAME 10/18, DELTAFILL 18, DELTAXSFT 10, GALAXY G3 FILL/XSFT STRETCH RESISTANT MICROCOIL DELIVERY SYSTEMS |
CODMAN & SHURTLEFF, INC. |
| K122263 |
07/27/2012 |
14.5-16.0 FRENCH CUFFED CATHETER REMOVAL DEVICE, SYMMETRY SURGICAL SINGEL USE |
SYMMETRY MEDICAL |
| K142429 |
08/29/2014 |
CODMAN Microcoil Delivery System, DELTAMAXX Microcoil Delivery System, ORBIT GALAXY G2 Microcoil Delivery System, EnPower Control Cable, Connector Cable |
Codman & Shurtleff, Inc |
| K133625 |
11/26/2013 |
AGILITY 10 STANDARD & SOFT 0.01IN. X 195CM, AGILITY 14 STANDARD & SOFT 0.014IN X 205CM & XL 350CM, AGILITY 16 STANDARD & |
Codman & Shurtleff, Inc. |
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