Medical Device Manufacturer · US , Mchenry , IL

Teca, Inc. - FDA 510(k) Cleared Devices

29 submissions · 29 cleared · Since 1976

Recent clearances: EEG ELECTRODES, SAPPHIRE SERIES 1P, 1L, 2L, AND 2ME, EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH

Total

Cleared

Denied

Teca, Inc. has 29 FDA 510(k) cleared neurology devices. Based in Mchenry, US.

Historical record: 29 cleared submissions from 1976 to 1996.

Browse the complete list of FDA 510(k) cleared neurology devices from this manufacturer. Filter by specialty or product code using the sidebar.

Teca, 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 - Teca, Inc.

29 devices

1-12 of 29

SAPPHIRE SERIES 1P, 1L, 2L, AND 2ME

K903731 · GWF

Neurology · 172d

Cleared Nov 15, 1990

EE1114, 1118, 1121 ELECTRO-ENCEPHALOGRAPH

K903004 · GWQ

Neurology · 129d

Cleared Feb 16, 1990

P460, DG32 ELECTROENCEPHALOGRAPH

TECA NEUROMAPPER 1620, BRAIN MAPPER

K894088 · OLT

Neurology · 160d

Cleared Mar 23, 1989

TECA 1A96, 1A97 AND 1A98 ELECTROENCEPHALOGRAPHS

K890881 · GWQ

Neurology · 30d

Cleared Feb 23, 1989

TECA/MEDELEC 'CONCEPT' P420

TECA/MEDELEC TTT THERMAL THRESHOLD TESTER

K872931 · LLN

Neurology · 112d

Cleared Feb 04, 1987

TECA/MEDELEC AS-10 SENSOR

K862906 · GWJ

Neurology · 188d

Cleared Feb 03, 1987

TECA/MEDELEC AUDIOSTAR

K863156 · GWJ

Neurology · 169d

Teca, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Teca, Inc.

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