Medical Device Manufacturer · US , Walker , MI

Biomedical Life Systems, Inc. - FDA 510(k) Cleared Devices

35 submissions · 35 cleared · Since 1984

Total

Cleared

Denied

Biomedical Life Systems, Inc. has 35 FDA 510(k) cleared neurology devices. Based in Walker, US.

Historical record: 35 cleared submissions from 1984 to 2018.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Biomedical Life Systems, Inc.

35 devices

1-12 of 35

ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS06-1

COMBINATION POWERED ELECTRICAL MUSCLE STIMULATOR AND INTERFERENTIAL...

K041388 · GZJ

Neurology · 182d

Cleared Jul 07, 2004

INTERFERENTIAL STIMULATOR, MODEL BMLS02-6

Physical Medicine · 273d

Cleared Apr 29, 2004

INTERFERENTIAL STIMULATOR, MODEL BMLS03-6

K040824 · LIH

Neurology · 30d

Cleared Mar 23, 2004

HIGH VOLTAGE PULSED STIMULATOR, MODEL BMLS02-7

K040306 · IPF

Physical Medicine · 43d

Cleared Jan 15, 2004

ELECTRO-NERVE STIMULATOR TENS, MODEL BMLS03-5

K033455 · GZJ

Neurology · 77d

Cleared Aug 19, 2003

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS03-1

K031427 · IPF

Physical Medicine · 105d

Cleared Feb 13, 2003

ELECTRO NEUROMUSCULAR STIMULATOR, MODEL BMLS02-5

K021588 · IPF

Physical Medicine · 275d

Biomedical Life Systems, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Biomedical Life Systems, Inc.

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