Medical Device Manufacturer · US , Mchenry , IL

Heyer Schulte Corp. - FDA 510(k) Cleared Devices

9 submissions · 9 cleared · Since 1976

Total

Cleared

Denied

Heyer Schulte Corp. has 9 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 9 cleared submissions from 1976 to 1979. Primary specialty: Neurology.

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

Heyer Schulte 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 - Heyer Schulte Corp.

9 devices

1-9 of 9

Cleared Nov 16, 1979

2 FR KELMAN CHAMBER MAINTAINER

K792096 · FMI

General Hospital · 29d

Cleared Aug 03, 1979

SUBCUTANEOUS TISSUE EXPANDER

K790842 · LCJ

General & Plastic Surgery · 93d

Cleared Sep 07, 1978

LUMBAR NERVE ROOT SHIELD

General Hospital · 35d

Cleared Oct 11, 1977

RADOVAN SUBCUTANEOUS TISSUE EXPANDER

K771224 · LCJ

General & Plastic Surgery · 98d

Cleared Nov 03, 1976

T-TUBE DRAIN, ROUND

K760778 · GCY

General & Plastic Surgery · 30d

Cleared Nov 01, 1976

MISHLER 2 CHAMB FLUSHING VALVE,STAND

K760784 · JXG

Neurology · 27d

Cleared Nov 01, 1976

MISHLER 2 CHAMB FLUSHING VALVE,ANTI-SYPH

K760785 · JXG

Neurology · 27d

Cleared Aug 30, 1976

VALVE, STANDARD MODEL PUDENZE FLUSHING

K760501 · JXG

Neurology · 7d

Heyer Schulte Corp. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Heyer Schulte Corp.

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