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.

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

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