Bio Protech, Inc.
FDA 510(k) medical device clearances.
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.