Pilling Weck Group is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Pilling Weck Group - FDA 510(k) Cleared Devices
5
Total
5
Cleared
0
Denied
Pilling Weck Group has 5 FDA 510(k) cleared medical devices. Based in Jeffrey, US.
Historical record: 5 cleared submissions from 1996 to 1997. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Pilling Weck Group Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Pilling Weck Group
5 devices
Cleared
Jun 11, 1997
PILLING WECK SECONDARY FLEXIBLE SLEEVE WITH TROCAR
General & Plastic Surgery
62d
Cleared
Mar 04, 1997
PILLING WECK 2 PIECE TAKE-APART INSTRUMENTS
Gastroenterology & Urology
70d
Cleared
Jan 10, 1997
SECONDARY TROCAR AND SLEEVE WITH INSUFFLATION PORT
Obstetrics & Gynecology
65d
Cleared
Dec 12, 1996
REUSABLE TROCAR WITH SLEEVE (COMMON)
General & Plastic Surgery
58d
Cleared
Nov 05, 1996
REUSABLE TROCAR WITH SLEEVE (COMMON)
General & Plastic Surgery
43d