FDA 510(k) Applications Submitted by GARY BUSSETT
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K040306 |
02/09/2004 |
HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7 |
BIOMEDICAL LIFE SYSTEMS, INC. |
K040824 |
03/30/2004 |
INTERFERENTIAL STIMULATOR, MODEL BMLS03-6 |
BIOMEDICAL LIFE SYSTEMS, INC. |
K041388 |
05/25/2004 |
COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1 |
BIOMEDICAL LIFE SYSTEMS, INC. |
K061476 |
05/30/2006 |
ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1 |
BIOMEDICAL LIFE SYSTEMS, INC. |
K102051 |
07/21/2010 |
PAIN BUDDY |
BIOMEDICAL LIFE SYSTEMS, INC. |
K172971 |
09/26/2017 |
BMLS16-1 |
BioMedical Life Systems, Inc. |
K042711 |
09/30/2004 |
MODEL BMLS03-7 |
BIOMEDICAL LIFE SYSTEMS, INC. |
K083441 |
11/20/2008 |
FREEDOM STIM 100 AND 200 ELECTRODE AND LEADWIRE EXTENSION |
MOTION MEDICAL PRODUCTS LLC |
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