John F. Greer Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
John F. Greer Co., Inc. - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
John F. Greer Co., Inc. has 5 FDA 510(k) cleared medical devices. Based in Oakland, US.
Historical record: 5 cleared submissions from 1986 to 1987. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by John F. Greer Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - John F. Greer Co., Inc.
5 devices
Cleared
Apr 17, 1987
E-Z LOOP
Gastroenterology & Urology
66d
Cleared
Apr 10, 1987
EZ TAC FILTER
Gastroenterology & Urology
63d
Cleared
Jan 14, 1987
E-Z HOLD - #4060
General Hospital
79d
Cleared
Dec 04, 1986
E-Z HOLD WITH ADHESIVE BASE.-#4065
Gastroenterology & Urology
38d
Cleared
Dec 04, 1986
ULTRA-GEL - #4083
Gastroenterology & Urology
38d