Medical Device Manufacturer · US , Edison , NJ

Lumiscope Co., Inc. - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 1988

Total

Cleared

Denied

Lumiscope Co., Inc. has 13 FDA 510(k) cleared medical devices. Based in Edison, US.

Historical record: 13 cleared submissions from 1988 to 2003.

Browse the FDA 510(k) cleared devices submitted by Lumiscope Co., Inc. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Lumiscope Co., Inc.

13 devices

1-13 of 13

Cleared Oct 22, 2003

CARDICARE MODEL MT-301F & MT-301C

K032714 · FLL

General Hospital · 50d

Cleared Jun 21, 1996

LUMISCOPE MODEL 2018 THERMOMETER

K954792 · FLL

General Hospital · 247d

Cleared Feb 23, 1994

INTERFERENTIAL CURRENT THERAPY UNIT

Physical Medicine · 266d

Physical Medicine · 122d

Cleared Aug 21, 1990

LUMISCOPE ALTERNATING PRESSURE PAD & PUMP

K901096 · FNM

General Hospital · 167d

LUMISCOPE ELECTRODES MODELS EL-08,11,15,06,21,25

K901809 · GXY

Neurology · 59d

Cleared Sep 06, 1989

LUMISCOPE MODEL 1000/APCC MODEL 1000

LUMISCOPE TENS MODEL 2000T OR APCC 3001 OR PAIN RE

K880452 · GZJ

Neurology · 51d

Lumiscope Co., Inc. - FDA 510(k) Cleared Devices

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