Medical Device Manufacturer · US , Mchenry , IL

Popper & Sons, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Popper & Sons, Inc. Gastroenterology & Urology ✕

2 devices

1-2 of 2

Cleared May 20, 1991

HYPODERMIC NEEDLES, SINGLE LUMEN

Gastroenterology & Urology · 52d

Cleared Mar 12, 1984

WESTERMAN-JENSEN BIOPSY NEEDLE

Gastroenterology & Urology · 56d