FDA 510(k) Applications Submitted by DAVID C FURR
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K040223 |
02/02/2004 |
POLYVAC INSTRUMENT DELIVERY SYSTEM |
SYMMETRY MEDICAL USA INC. |
| K140962 |
04/15/2014 |
NORMED VARIO SUBTALAR SCREW |
NORMED NEDIZIN TECHNIK GMBH |
| K130680 |
03/13/2013 |
ACRYTONE, REZEN NF, AND ISO FAST DENTURE RESINS |
DENTSOLL, INC. |
| K110898 |
03/30/2011 |
S.C.O.R.E.S. UNIT |
AMMED SURGICAL EQUIPMENT, LLC |
| K081820 |
06/27/2008 |
AVALON ELITE BI-CAVAL DUAL LUMEN CATHETER, 13FR, 16FR, 19FR, 20FR, 23FR, 27FR, 31FR |
AVALON LABORATORIES, LLC |
| K032119 |
07/09/2003 |
PARAGON MEDICAL SURGICAL INSTRUMENT DELIVERY SYSTEM VARIOUS |
PARAGON MEDICAL, INC. |
| K112599 |
09/07/2011 |
INSURGICAL SINGLE USE POWER EQUIPMENT |
INSURGICAL LLC |
| K132824 |
09/09/2013 |
CARESTREAM VUE PACS VERSION 11.4 CARESTREAM VUE MOTION APPLICATION |
CARESTREAM HEALTH,INC. |
| K093019 |
09/29/2009 |
ENAMELITE ACRYSEAL SPRAY SEALANT |
ENAMELITE LLC |
| K123177 |
10/09/2012 |
STIMLASE 2000 LOW LEVEL LASER THERAPY SYSTEM |
LASERSTIM, INC. |
| K123347 |
10/31/2012 |
NORMED ANKLE FIX SYSTEM 4.0 AND NORMED ANKLE FIX PLUS SYSTEM 4.0 |
NORMED MEDIZIN-TECHNIK GMBH |
| K134037 |
12/31/2013 |
PREMVIA |
BIOTIME, INC. |
|
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