Medical Device Manufacturer · US , Crofton , MD

Bhs Intl., Inc. - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 1994
2
Total
2
Cleared
0
Denied

Bhs Intl., Inc. has 2 FDA 510(k) cleared medical devices. Based in Crofton, US.

Historical record: 2 cleared submissions from 1994 to 2001. Primary specialty: Cardiovascular.

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

FDA 510(k) Regulatory Record - Bhs Intl., Inc.
2 devices
1-2 of 2
Cleared Mar 29, 2001
FINGER PULSE METER
K000814 · DQA
Anesthesiology · 381d
Cleared Apr 26, 1994
MANUAL STETOSCOPE
K940578 · LDE
Cardiovascular · 77d
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All2 Cardiovascular 1 Anesthesiology 1