American Heyer Schulte is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
American Heyer Schulte - FDA 510(k) Cleared Devices
13
Total
13
Cleared
0
Denied
American Heyer Schulte has 13 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 13 cleared submissions from 1980 to 1984. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by American Heyer Schulte Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - American Heyer Schulte
13 devices
Cleared
Jun 27, 1984
VENTRAL WALL DEFECT REDUCT SILO
General & Plastic Surgery
162d
Cleared
Apr 03, 1984
ONE-PIECE SHUNT
Neurology
96d
Cleared
Feb 03, 1984
RADOVAN SUBCUTANEOUS TISSUE EXPANDER
General & Plastic Surgery
121d
Cleared
Jan 25, 1984
AMER. V. MUELLER SURG. STAPLES ILA
General & Plastic Surgery
71d
Cleared
Dec 29, 1983
AMER. V. MUELLER SURGICALSTAPLES-CARTR
General & Plastic Surgery
72d
Cleared
Sep 29, 1983
HEYER-SCHULTE AFTERLOADING CATHETER
Radiology
48d
Cleared
Apr 28, 1983
VENTRICULAR ACCESS SYSTEM
General Hospital
133d
Cleared
Apr 12, 1983
CHEMOTHERAPY INFUSION CATHETER
General & Plastic Surgery
270d
Cleared
Aug 16, 1982
LARGE VOLUME CLOSED WOUND SUCTION DRAIN
General & Plastic Surgery
35d
Cleared
Feb 18, 1982
EXTERNAL VENTRICULAR DRAINAGE SYS.
Neurology
20d
Cleared
Jun 26, 1981
SPETZLER LUMBAR-PERITONEAL SYSTEM
Neurology
46d
Cleared
Dec 18, 1980
AMERICAN HEYER-SCHULTE LOW PROFILE VALVE
Neurology
59d