Rhythmlink International, LLC
FDA 510(k) medical device clearances.
Top product codes for Rhythmlink International, LLC
Recent clearances by Rhythmlink International, LLC
- K203079 — MR Conditional Sticky Pad Electrode
- K200984 — Guardian Needle Electrode
- K191225 — EEG Electrode Template
- K190801 — PressOn Electrode Headset
- K172503 — MR Conditional Cup Electrode, MR Conditional Webb Electrode
- K132138 — RHYTHMLINK DISPOSABLE CONCENTRIC STIMULATING PROBE
- K130220 — MR CONDITIONAL PRESSON ELECTRODE
- K130287 — MR CONDITIONAL CUP ELECTRODE, MR CONDITIONAL WEBB ELECTRODE
- K121347 — PRESSON ELECTRODE
- K120342 — EMG RECORDING ELECTRODE ASSEMBLY
- K112435 — RHYTHMLINK MONOPOLAR STIMULATING INSTRUMENT
- K103200 — PROPEP DELIVERY DEVICE
- K091055 — RHYTHMLINK DISPOSABLE CONCENTRIC EMG NEEDLE, MODEL D039032252R
- K091056 — RHYTHMLINK DISPOSABLE MONOPOLAR EMG NEEDLE, MODEL TFDN26032252R
- K072736 — RHYTHMLINK INTERNATIONAL MONOPOLAR STIMULATING INSTRUMENT
- K061148 — RHYTHMLINK DISC ELECTRODES
- K052188 — CUTANEOUS ELECTRODE
- K022914 — RHYTHMLINK INTERNATIONAL SUBDERMAL NEEDLE ELECTRODES
Data sourced from openFDA. This site is unofficial and independent of the FDA.