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

Popper & Sons, Inc. has 8 FDA 510(k) cleared medical devices. Based in Mchenry, US.

Historical record: 8 cleared submissions from 1984 to 1991. Primary specialty: General & Plastic Surgery.

Browse the FDA 510(k) cleared devices submitted by Popper & Sons, Inc. Filter by specialty or product code using the sidebar.

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

8 devices

1-8 of 8

Cleared May 20, 1991

HYPODERMIC NEEDLES, SINGLE LUMEN

Gastroenterology & Urology · 52d

Cleared Oct 26, 1984

J -JAMSHIDI TYPE-BONE MARROW BIOPSY/ASPI

General & Plastic Surgery · 25d

Cleared Oct 25, 1984

ILLINOIS STERNUM/ILIAC ASPIRATION NEEDLE

General & Plastic Surgery · 36d

Cleared Aug 09, 1984

WESCOTT TYPE BIOPSY NEEDLE

General & Plastic Surgery · 51d

Cleared Jun 05, 1984

ANTRUM NEEDLE-WOLF TYPE

Orthopedic · 67d

Cleared Jun 05, 1984

GARDNER TYPE BONE MARROW NEEDLE

General & Plastic Surgery · 67d

Cleared May 02, 1984

BIERMAN BIOPSY NEEDLE

General & Plastic Surgery · 33d

Cleared Mar 12, 1984

WESTERMAN-JENSEN BIOPSY NEEDLE

Gastroenterology & Urology · 56d