Microvasive is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Microvasive - FDA 510(k) Cleared Devices
18
Total
18
Cleared
0
Denied
Microvasive has 18 FDA 510(k) cleared gastroenterology & urology devices. Based in Mchenry, US.
Historical record: 18 cleared submissions from 1983 to 1987.
Browse the complete list of FDA 510(k) cleared gastroenterology & urology devices from this manufacturer. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Microvasive
18 devices
Cleared
Oct 09, 1987
LOW PROFILE GASTROSTOMY
Gastroenterology & Urology
87d
Cleared
Apr 17, 1987
THERMAL COAGULATOR
Gastroenterology & Urology
56d
Cleared
Dec 16, 1986
JEJUNAL FEEDING TUBE
Gastroenterology & Urology
252d
Cleared
Dec 16, 1986
REPLACEMENT GASTROSTOMY TUBE
Gastroenterology & Urology
252d
Cleared
Apr 07, 1986
CHALLENGER HOT BIOPSY FORCEPS
Gastroenterology & Urology
63d
Cleared
Apr 07, 1986
INFLATOR/DEFLATOR PISTON SYRINGE
Gastroenterology & Urology
47d
Cleared
Nov 13, 1985
NEEDLE W/STYLET FOR IMPLANTATION
General & Plastic Surgery
23d
Cleared
Oct 25, 1985
MICROVASIVE SILICONE SPRAY
General Hospital
21d
Cleared
Jun 24, 1985
PAPILLOTOME
Gastroenterology & Urology
63d
Cleared
Jun 04, 1985
FLEXIBLE FIBEROPTIC ENDOSCOPE
Gastroenterology & Urology
123d
Cleared
Jan 15, 1985
RIGID FIBEROPITC ENDOSCOPE
Gastroenterology & Urology
39d
Cleared
May 22, 1984
GASTROSTOMY FEEDING TUBE
Gastroenterology & Urology
50d
Cleared
Apr 20, 1984
DRAINAGE STENT
Gastroenterology & Urology
122d
Cleared
Apr 05, 1984
HYPODERMIC NEEDLES & STYLETS
General Hospital
91d
Cleared
Feb 17, 1984
SPECIMEN TRAP
General Hospital
59d
Cleared
Nov 28, 1983
ENDOSCOPIC RETROGRADE
Gastroenterology & Urology
56d
Cleared
Nov 14, 1983
MUTO BRUSH
Gastroenterology & Urology
48d
Cleared
Nov 14, 1983
ASPIRATION & IRRIGATION CATHETER
Gastroenterology & Urology
48d