FDA 510(k) Applications Submitted by RUSS PAGANO
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030349 |
02/03/2003 |
HEALTHOMETER PROFESSIONAL BODY FAT MONITOR AND SCALE, MODELS BFM 940, BFM 945 & BFM 960 |
BONSO ELECTRONICS INTERNATIONAL INC. |
K061111 |
04/21/2006 |
TINNITUS PHASE-OUT |
TINNITUS CONTROL, INC. |
K031624 |
05/23/2003 |
TINNITUS RX |
TINNITUS CONTROL, INC. |
K032160 |
07/15/2003 |
ARTELON SURGICAL SUTURE |
ARTIMPLANT AB |
K032866 |
09/15/2003 |
CLARITY PET |
SHARED P.E.T. IMAGING, LLC |
K042692 |
09/30/2004 |
CLARITY FUSION |
SHARED P.E.T. IMAGING, LLC |
K061954 |
07/11/2006 |
ARTELON CMC SPACER ARTHRO |
ARTIMPLANT AB |
K061956 |
07/11/2006 |
ARTELON STT SPACER |
ARTIMPLANT AB |
K013094 |
09/17/2001 |
ORTHOSONIX ENERGEX |
ORTHOSONIX, INC. |
K023575 |
10/24/2002 |
CONCERT CRANIOPLAST |
IMMEDICA, INC. |
K063343 |
11/06/2006 |
BIOPTIGEN SPECTRAL DOMAIN OPHTHALMIC IMAGING SYSTEM |
BIOPTIGEN, INC. |
K013755 |
11/13/2001 |
CONCERT RADIOPAQUE BONE CEMENT |
IMMEDICA, INC. |
K043195 |
11/18/2004 |
NEO IMPLANT SYSTEM |
NEOSS LTD |
K213974 |
12/20/2021 |
GEM FLOW COUPLER Monitor (GEM1020M-2) |
Synovis Micro Companies Alliance, Inc. |
|
|