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.
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