Medical Device Manufacturer · US , Spencer , IN

Biomedix, Inc. - FDA 510(k) Cleared Devices

11 submissions · 11 cleared · Since 1993

Total

Cleared

Denied

Biomedix, Inc. has 11 FDA 510(k) cleared medical devices. Based in Spencer, US.

Historical record: 11 cleared submissions from 1993 to 2014.

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

FDA 510(k) Regulatory Record - Biomedix, Inc.

11 devices

1-11 of 11

Cleared Aug 29, 2014

SELEC-3 I.V.ADMINISTRATION SET

K142097 · FPA

General Hospital · 28d

Q.STEPS BIOMETER G/C DUAL MONITORING SYSTEM

Q.STEPS BIOMETER G BLOOD GLUCOSE MONITORING SYSTEM

K033627 · CGA

Chemistry · 184d

Cleared Dec 29, 1997

FLOSTAT VASCULAR REPORT GENERATOR (VRG)

BIOMEDIX I.V. EXTENSION LINE W/ STOPCOCK MODEL B50-102/B51-102

K961928 · FPA

General Hospital · 122d

Cleared Sep 27, 1993

SELEC-3

K925645 · FPA

General Hospital · 322d

Biomedix, Inc. - FDA 510(k) Cleared Devices

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