Biomedix, Inc.
Biomedix, Inc. holds FDA 510(k) medical device clearances, first cleared 1993, most recent 2014, with 1 FDA device recall on record.
Top product codes for Biomedix, Inc.
FDA recalls by Biomedix, Inc.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Biomedix, Inc.
- K142097 — SELEC-3 I.V.ADMINISTRATION SET
- K122281 — PADNET 2.0
- K073146 — PADNET+
- K050182 — Q.STEPS BIOMETER G/C DUAL MONITORING SYSTEM
- K042616 — BIOMEDIX PADNET LAB
- K033627 — Q.STEPS BIOMETER G BLOOD GLUCOSE MONITORING SYSTEM
- K973857 — FLOSTAT VASCULAR REPORT GENERATOR (VRG)
- K973644 — FLOSTAT VASCULAR LAB
- K961928 — BIOMEDIX I.V. EXTENSION LINE W/ STOPCOCK MODEL B50-102/B51-102
- K925645 — SELEC-3
- K926498 — ENDOGRIP
Data sourced from openFDA. This site is unofficial and independent of the FDA.