Medical Device Manufacturer · US , Sparks , MD

Bionicare Medical Technologies, Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2003
2
Total
2
Cleared
0
Denied

Bionicare Medical Technologies, Inc. has 2 FDA 510(k) cleared medical devices. Based in Sparks, US.

Historical record: 2 cleared submissions from 2003 to 2005. Primary specialty: Neurology.

Browse the FDA 510(k) cleared devices submitted by Bionicare Medical Technologies, Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Bionicare Medical Technologies, Inc.

2 devices
1-2 of 2
Cleared Dec 05, 2005
BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
K052625 · NYN
Neurology · 73d
Cleared Jun 06, 2003
MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000
K030332 · NYN
Neurology · 126d
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