Rhythmlink International, LLC
Rhythmlink International, LLC holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2021.
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.