Atlas FDA

PLASMAT SECURA HEPARIN-INDUCED EXTRACORPOREAL LDL APHERESIS SYSTEM (H.E.L.P.)

FDA premarket approval P940016/S012 · decided 2009-04-20

Approval details

PMA number
P940016
Supplement
S012
Supplement type
Real-Time Process
Supplement reason
Change Design/Components/Specifications/Material
Trade name
PLASMAT SECURA HEPARIN-INDUCED EXTRACORPOREAL LDL APHERESIS SYSTEM (H.E.L.P.)
Generic name
Lipoprotein, low density, removal
Applicant
B. Braun Avitum AG
Date received
2009-02-19
Decision date
2009-04-20
Days to decision
60 days
Decision code
APPR
Product code
MMY
Advisory committee
Gastroenterology, Urology
Expedited review
No
Location
Melsungen
Statement
APPROVAL FOR A CHANGE TO THE PACKAGING MATERIAL IN THE POUCH USED FOR THE HEPARIN ADSORBER COMPONENT OF THE DEVICE.

Class III intelligence, same tools

PMAs share the API, exports and alerts with 510(k) data - watch an applicant and hear about every approval.

510(k) clearances by this applicant

RecordFirmDate
Diacap Pro Dialyzer (K170574)B. Braun Avitum AG2017-08-11
xevonta dialyzer (K143482)B. Braun Avitum AG2016-03-01
SOLCART B (K102194)B. Braun Avitum AG2011-04-25
DIACAP POLYSULFONE HIFLO 23 HEMODILAYZER , MODEL 72036811 (K100334)B. Braun Avitum AG2010-04-22
DIALOG WITH ADIMEA OPTION (K083460)B. Braun Avitum AG2010-02-18