Chartermed, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Chartermed, Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Chartermed, Inc. has 4 FDA 510(k) cleared medical devices. Based in Lakewood, US.
Historical record: 4 cleared submissions from 1990 to 1997. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Chartermed, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Chartermed, Inc.
4 devices
Cleared
Nov 24, 1997
CHARTERMED TPN-EVA BAGS
General Hospital
97d
Cleared
Oct 29, 1990
ADMIXTURE CONTAINER FOR TOTAL PARENTERAL NUTRITION
General Hospital
174d
Cleared
Aug 30, 1990
CHARTERMED EMPTY TPN CONTAINER - 100 ML CAPACITY
General Hospital
87d
Cleared
Jun 01, 1990
600 OR 1200 ML. ENTERAL BAG ADMINISTRATION SET
Gastroenterology & Urology
46d