Panamedix, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Panamedix, Inc. - FDA 510(k) Cleared Devices
6
Total
6
Cleared
0
Denied
Panamedix, Inc. has 6 FDA 510(k) cleared medical devices. Based in Costa Mesa, US.
Historical record: 6 cleared submissions from 1986 to 1988. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Panamedix, Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Panamedix, Inc.
6 devices
Cleared
Feb 03, 1988
NUTRITION DELIVERY SETS FOR VM 05 AMBULA. PUMP
Gastroenterology & Urology
267d
Cleared
Jul 21, 1987
TWO FLUID W/CHECK VALVE
General Hospital
70d
Cleared
Jun 24, 1987
THREE FLUID I.V. SETS
General Hospital
43d
Cleared
Jun 24, 1987
TWO FLUID I.V. SETS
General Hospital
43d
Cleared
Feb 10, 1987
GRASEBY PCAS MODEL NO. 0124-0701, PVS DYTINHR PUMP
General Hospital
48d
Cleared
Dec 16, 1986
LOW VOLUME EXTENSION SET
General Hospital
40d