Biomedix, Inc. is one of 18577 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Biomedix, Inc. - FDA 510(k) Cleared Devices
Recent clearances: SELEC-3 I.V.ADMINISTRATION SET, PADNET 2.0, PADNET+
11
Total
11
Cleared
0
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.
510(k) submissions have been managed by Tuv America, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Biomedix, Inc.
11 devices
Cleared
Aug 29, 2014
SELEC-3 I.V.ADMINISTRATION SET
General Hospital
28d
Cleared
Aug 29, 2012
PADNET 2.0
Cardiovascular
30d
Cleared
Nov 21, 2007
PADNET+
Cardiovascular
13d
Cleared
Aug 09, 2005
Q.STEPS BIOMETER G/C DUAL MONITORING SYSTEM
Chemistry
194d
Cleared
Oct 12, 2004
BIOMEDIX PADNET LAB
Cardiovascular
19d
Cleared
May 21, 2004
Q.STEPS BIOMETER G BLOOD GLUCOSE MONITORING SYSTEM
Chemistry
184d
Cleared
Dec 29, 1997
FLOSTAT VASCULAR REPORT GENERATOR (VRG)
Radiology
81d
Cleared
Dec 23, 1997
FLOSTAT VASCULAR LAB
Radiology
90d
Cleared
Sep 16, 1996
BIOMEDIX I.V. EXTENSION LINE W/ STOPCOCK MODEL B50-102/B51-102
General Hospital
122d
Cleared
Sep 27, 1993
SELEC-3
General Hospital
322d
Cleared
Apr 07, 1993
ENDOGRIP
Anesthesiology
99d