Lumiscope Co., Inc.
Lumiscope Co., Inc. holds FDA 510(k) medical device clearances, first cleared 1988, most recent 2003.
Top product codes for Lumiscope Co., Inc.
Recent clearances by Lumiscope Co., Inc.
- K032714 — CARDICARE MODEL MT-301F & MT-301C
- K954792 — LUMISCOPE MODEL 2018 THERMOMETER
- K931768 — INTERFERENTIAL CURRENT THERAPY UNIT
- K925054 — INFRARED LAMP
- K924081 — LUMISONIC
- K920099 — GYMMAN
- K901849 — LUMISCOPE EMS 8000
- K901096 — LUMISCOPE ALTERNATING PRESSURE PAD & PUMP
- K901726 — LUMISCOPE MICRO 100
- K901809 — LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25
- K894127 — LUMISCOPE MODEL 1000/APCC MODEL 1000
- K884722 — LUMINEB I
- K880452 — LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE
Data sourced from openFDA. This site is unofficial and independent of the FDA.