Rd Medical Mfg., Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Rd Medical Mfg., Inc. - FDA 510(k) Cleared Devices
4
Total
4
Cleared
0
Denied
Rd Medical Mfg., Inc. has 4 FDA 510(k) cleared medical devices. Based in Culebra, US.
Historical record: 4 cleared submissions from 1999 to 2001. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Rd Medical Mfg., Inc. Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Rd Medical Mfg., Inc.
4 devices
Cleared
Mar 30, 2001
PARSET NEEDLELESS PRIMARY SET FOR BLUNT CANNULA, A10003E, PARSET NEEDLELESS...
General Hospital
35d
Cleared
Apr 20, 2000
PARSET PRIMARY SET WITH CHECK VALVE, MODEL A10002E
General Hospital
15d
Cleared
Feb 10, 2000
PARSET SECONDARY ADMINISTRATION SET, LUERLOCK, MODEL A14001E, PARSET...
General Hospital
38d
Cleared
Aug 23, 1999
PARSET, MODEL A10001E
General Hospital
62d