Chathamborough Research Group, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chathamborough Research Group, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Chathamborough Research Group, Inc. has 4 FDA 510(k) cleared medical devices. Based in Pittsboro, US.
Historical record: 4 cleared submissions from 1986 to 1992. Primary specialty: General & Plastic Surgery.
Browse the FDA 510(k) cleared devices submitted by Chathamborough Research Group, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chathamborough Research Group, Inc.
4 devices
Cleared
Sep 11, 1992
SPLATTER SHIELD
General Hospital
267d
Cleared
Dec 24, 1990
SHARPOINT POLYPROPYLENE NONABSORB SURG SUTURES USP
General & Plastic Surgery
60d
Cleared
Aug 17, 1990
PARKER MICROPUMP MODEL 2100
General Hospital
86d
Cleared
Sep 30, 1986
SHARPOINT STAINLESS STEEL SUTURE
General & Plastic Surgery
50d