Biomedical Life Systems, Inc.

FDA Regulatory Profile

Summary

Total Recalls
0
510(k) Clearances
37
Inspections
4
Compliance Actions
0

Recent 510(k) Clearances

K-NumberDeviceDate
K172971BMLS16-1July 8, 2018
K102051PAIN BUDDYJuly 29, 2011
K061476ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1July 26, 2006
K042711MODEL BMLS03-7March 14, 2005
K041388COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL STIMULATOR, MODEL BMLS04-1November 23, 2004
K040007INTERFERENTIAL STIMULATOR, MODEL BMLS02-6July 7, 2004
K033174BMLS03-3June 30, 2004
K040824INTERFERENTIAL STIMULATOR, MODEL BMLS03-6April 29, 2004
K040306HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7March 23, 2004
K033455ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5January 15, 2004
K031427ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1August 19, 2003
K021588ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS02-5February 13, 2003
K021271ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-3February 6, 2003
K021270ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-2February 6, 2003
K022925ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-10November 19, 2002
K022841ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS02-9November 19, 2002
K020712ELECTRO-NERVE STIMULATOR TENS MODEL BMLS02-4September 24, 2002
K010749ELECTRO NEUROMUSCULAR STIMULATOR, MODEL NMS-DIGITALSeptember 28, 2001
K010209ELECTRO-NERVE STIMULATOR TENS, MODEL HE-DIGITALJune 12, 2001
K990230ELECTRO-NERVE STIMULATOR TENS, MODEL LXAugust 19, 1999