Medegen Medical Manufacturing Services is one of 16278 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Medegen Medical Manufacturing Services - FDA 510(k) Cleared Devices
Recent clearances: MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL, TRU-SWAB STOCOCK, DRUG ACCESS SPIKE
4
Total
4
Cleared
0
Denied
Medegen Medical Manufacturing Services has 4 FDA 510(k) cleared medical devices. Based in Trabuco Canyon, US.
Historical record: 4 cleared submissions from 2005 to 2008. Primary specialty: General Hospital.
Browse the FDA 510(k) cleared devices submitted by Medegen Medical Manufacturing Services Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Regulatory Technology Services, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Medegen Medical Manufacturing Services
4 devices
Cleared
Dec 30, 2008
MAXGUARD ADVANCED LUER ACTIVATED DEVICE WITH ANTIMICROBIAL
General Hospital
12d
Cleared
Sep 09, 2005
TRU-SWAB STOCOCK
General Hospital
14d
Cleared
Aug 16, 2005
DRUG ACCESS SPIKE
General Hospital
34d
Cleared
Jun 22, 2005
INTRAVASCULAR ADMINISTRATION SET AND EXTENSION SET
General Hospital
15d