Medical Device Manufacturer · US , Mchenry , IL

Britt Corp., Inc. - FDA 510(k) Cleared Devices

17 submissions · 16 cleared · Since 1979

Total

Cleared

Denied

Britt Corp., Inc. has 16 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 16 cleared submissions from 1979 to 2001.

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

FDA 510(k) Regulatory Record - Britt Corp., Inc.

17 devices

1-12 of 17

Cleared May 18, 2001

VASO PRESS DVT FOOT GARMENT #VP 520

K003828 · JOW

Cardiovascular · 158d

Cleared Jun 22, 2000

VASO PRESS DVT SYSTEM, MODELS VP500, VP501

K991038 · JOW

Cardiovascular · 451d

Cleared Mar 19, 1999

VASO PRESS SYSTEM

K974393 · JOW

Cardiovascular · 483d

Cleared Oct 16, 1986

MODEL 545-45 FOR NEUROLOGICAL SURGICAL APPLICATION

K860977 · LLF

Neurology · 216d

Cleared Jul 18, 1986

MODEL 545-45 LASER FOR EAR, NOSE & THROAT

K860975 · EWG

Ear, Nose, Throat · 126d

Cleared Jul 07, 1986

MODEL 545-45 LASER FOR DERMA., POD., SURGICAL

K860974 · GEX

General & Plastic Surgery · 115d

Cleared May 06, 1986

MODEL 525-25 WATT C02 LASER FOR EAR, NOSE & THROAT

K860277 · EWG

Ear, Nose, Throat · 99d

Cleared Apr 23, 1986

MODEL 525 - 25 WATT CO2 MEDICAL LASER/PODIATRY

K860273 · GEX

General & Plastic Surgery · 86d

Cleared Apr 15, 1986

MODEL 525-25 WATT CO2 LASER FOR DERMA/PLASTIC

K860278 · GEX

General & Plastic Surgery · 78d

Cleared Nov 12, 1985

MODEL J25-25 WATT CO2 LASER

K851425 · HHR

Obstetrics & Gynecology · 216d

Cleared Oct 26, 1984

FITNESS LOGGER

K840020 · DPS

Cardiovascular · 295d

Cleared Oct 26, 1984

FITEX

K840036

Physical Medicine · 295d

Britt Corp., Inc. - FDA 510(k) Cleared Devices

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