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. General & Plastic Surgery ✕

5 devices

1-5 of 5

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

GARDNER TYPE BONE MARROW NEEDLE

General & Plastic Surgery · 67d

Cleared May 02, 1984

BIERMAN BIOPSY NEEDLE

General & Plastic Surgery · 33d