Medical Device Manufacturer · US , Mchenry , IL

Nemectron Medical, Inc. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 1980

Total

Cleared

Denied

Nemectron Medical, Inc. has 12 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 12 cleared submissions from 1980 to 1993. Primary specialty: Physical Medicine.

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

Nemectron Medical, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Nemectron Medical, Inc.

13 devices

1-12 of 13

Cleared May 26, 1993

THERMODYN

K923396 · IRT

Physical Medicine · 320d

Cleared Jul 27, 1990

NEMECTRON MICROWAVE

K895000 · IOA

Physical Medicine · 353d

Cleared Jul 23, 1986

NEMECTROSON MODEL 2

K862376 · IMJ

Physical Medicine · 29d

Cleared Mar 10, 1986

NEMECTRODYN MODEL 2 & ENDOVAC 2 POWER MUSCLE STIM.

K854720 · IPF

Physical Medicine · 108d

Cleared Mar 06, 1986

NEMECTRODYN MODEL 2 & ENDOVAC 2

Physical Medicine · 118d

Cleared Oct 25, 1984

NEMDI

K843734 · KCX

General & Plastic Surgery · 31d

Cleared Oct 25, 1984

SOFTEPIL

K843735 · KCX

General & Plastic Surgery · 31d

Cleared Mar 31, 1983

EMG BIOFEEDBACK DEVICE

K823511 · HCC

Neurology · 122d

Cleared Mar 15, 1982

NEMECTRODYN MODELS 8,7,5 (VOLS. I-IV

K820334

Neurology · 38d

Cleared May 11, 1981

ELECTRODYN CII-INTERFERENTIAL MUSCLE

K810513 · IPF

Physical Medicine · 76d

Cleared Mar 16, 1981

NEMECTRODYN 8

K802804 · IPF

Physical Medicine · 131d

Nemectron Medical, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Nemectron Medical, Inc.

Filters