FDA 510(k) Applications Submitted by Ed Horton
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K980210 |
01/21/1998 |
VARIOUS SURGICAL OR PATIENT DRAPES |
GEL-LITE, L.L.C. |
| K240404 |
02/09/2024 |
NovaBone Putty - Bioactive Synthetic Bone Graft (NB6600, NB6610, NB6615) |
NovaBone Products, LLC |
| K220498 |
02/22/2022 |
NovoGen Wound Matrix |
Novabone Products, LLC |
| K081259 |
05/02/2008 |
DDU-2300 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K131525 |
05/28/2013 |
SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K121853 |
06/25/2012 |
DDU-2400/2450 SEMIAUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
| K141809 |
07/07/2014 |
RMU-1000 AUTOMATED CHEST COMPRESSION SYSTEM |
DEFIBTECH, LLC |
| K242299 |
08/02/2024 |
NovaBone Putty - Synthetic Bioactive Bone Graft |
NovaBone Products, LLC |
| K113787 |
12/22/2011 |
DDU-120 FULLY AUTOMATIC EXTERNAL DEFIBRILLATOR AND ACCESSORIES |
DEFIBTECH, LLC |
|
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