Emg Technology Co., Ltd.
Emg Technology Co., Ltd. holds FDA 510(k) medical device clearances, first cleared 2003, most recent 2011, with 1 FDA device recall on record.
Top product codes for Emg Technology Co., Ltd.
FDA recalls by Emg Technology Co., Ltd.
Recalls are matched by FDA's recalling-firm name — openFDA's enforcement dataset doesn't reference 510(k) numbers, so a recall here may cover devices beyond this company's 510(k) clearances.
Recent clearances by Emg Technology Co., Ltd.
- K112421 — EMG SUCTION UNIT
- K072634 — EMG TRITON -COMP,MODEL NCA01-XXX SERIES
- K063448 — EMG AC/DC SUCTION UNIT
- K062888 — MIDDLE WHEEL DRIVE POWER CHAIR, CWD01
- K052438 — EMG HANDLE NEBULIZER NB02 SERIES
- K043520 — EMG CTA01-XXX SERIES PURO OXYGEN CONCENTRATOR
- K043238 — COMPRESSOR NEBULIZER, MODEL EMG NBA02-XXX SERIES
- K042349 — EMG MODEL SUA01 SUCTION UNIT
- K033206 — EPW FOLDABLE POWER WHEELCHAIR, EPW-03
- K033204 — ESG 4-WHEEL SCOOTER, ESG-03
- K023148 — EPW POWERED WHEELCHAIR, GP-201
Data sourced from openFDA. This site is unofficial and independent of the FDA.