Medical Device Manufacturer · US , Mchenry , IL

Birtcher Corp. - FDA 510(k) Cleared Devices

27 submissions · 27 cleared · Since 1976

Total

Cleared

Denied

Birtcher Corp. has 27 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 27 cleared submissions from 1976 to 1988. Primary specialty: General & Plastic Surgery.

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

Birtcher Corp. 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 - Birtcher Corp.

27 devices

1-12 of 27

BIRT-A-SWITCH, DSP PUSH BUTTON, MODEL NO. 768

K860687 · GEI

General & Plastic Surgery · 27d

Cleared Mar 24, 1986

ELECTROSURGERY PENCIL, MODEL 767

K860718 · GEI

General & Plastic Surgery · 26d

Cleared Jan 13, 1986

SURGICAL CAUTERIES MODELS 775-11,12,13,31,32 & 33

K854814 · GEI

General & Plastic Surgery · 41d

Cleared Dec 24, 1985

BI-POLAR FORCEPS

K854864 · GEI

General & Plastic Surgery · 19d

Cleared May 20, 1985

ELECTROSURGICAL UNIT 774

K850668 · GEI

General & Plastic Surgery · 89d

Cleared May 20, 1985

MODEL 775 BIPOLAR COAGULATOR

K850943 · GEI

General & Plastic Surgery · 74d

Cleared Apr 09, 1985

CARDIO-NEC MODEL 365

K844101 · DPS

Cardiovascular · 168d

Cleared Mar 06, 1985

CARDIO ANALYZER MODEL 380

K844104 · LOS

Cardiovascular · 134d

Cleared Feb 28, 1985

ELECTROSURGICAL PENCIL HOLDER 720

K850297 · GEI

General & Plastic Surgery · 35d

Cleared Jan 18, 1985

CARDIOPAC DEFIBRILLATOR 444

Physical Medicine · 8d

Birtcher Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Birtcher Corp.

Filters