Greenwald Surgical Co., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Greenwald Surgical Co., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Greenwald Surgical Co., Inc. has 4 FDA 510(k) cleared medical devices. Based in Mchenry, US.
Historical record: 4 cleared submissions from 1978 to 1994. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Greenwald Surgical Co., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Greenwald Surgical Co., Inc.
4 devices
Cleared
Apr 01, 1994
GREENWALD CONTROL-TIP CYSTOSCOPIC ELECTRODE
Gastroenterology & Urology
276d
Cleared
Apr 01, 1994
GREENWALD FLEXIBLE ENDOSCOPIC ELECTRODE
Gastroenterology & Urology
276d
Cleared
Apr 01, 1994
GREENWALD CONTROL TIP URETEROSCOPIC ELECTRODE
Gastroenterology & Urology
276d
Cleared
Apr 28, 1978
CLAMP, INCONTINENCE, BAUMRUCKER
Gastroenterology & Urology
93d