Bio Protech, Inc.
Bio Protech, Inc. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2019.
Top product codes for Bio Protech, Inc.
Recent clearances by Bio Protech, Inc.
- K192035 — EvaQMax Smoke Evacuation System
- K152984 — Disposable Concentric Needle electrodes, Disposable Monopolar Needle electrodes, Disposable EP Needle electrodes, Disposable Hypodermic Needle electrodes
- K153019 — Disposable Adhesive Surface Electrodes, Disposable/Reusable Cup Electrodes
- K143103 — PROPENCIL Smoke Pencil
- K142099 — CUTANEOUS ELECTRODES
- K111270 — REUSABLE STIMULATING ELECTRODES
- K100246 — MAX-IF1000
- K091248 — MAXEMS, MODELS 1000 AND 2000
- K092732 — PROPENCIL ESU PENCIL
- K092761 — PROPLATE, MODELS 9641C, 9641F, P9641C, P9641F, 9642C, 9642F AND P9642C
- K083148 — TELECTRODE WET GEL ECG ELECTRODE
- K073438 — PROSTIM 1000/2000
- K073360 — PROPLATE
- K053011 — PRO-NEO NEONATAL ECG ELECTRODE, MODELS SG15 AND SR20
- K042301 — PROTENS ELECTRODE
- K040784 — PROTAB ECG TABB ELECTRODE
- K020003 — ELECTROCARDIOGRAPH (ECG) ELECTRODE, NON-STERILE
Data sourced from openFDA. This site is unofficial and independent of the FDA.