Skip to content
FDA.report
Public FDA data
NDC
RxNorm
DailyMed
Applications
GUDID
GMDN
PMA
PMN
MAUDE
Recalls
Search FDA.report
Search
Home
Company-Registration
1018216636
Device Listing 1018216636
Listing Summary
#
Listing key
1018216636
Premarket submission
K082150
Device
MODIFICATION TO PAXGENE BLOOD RNA SYSTEM
Applicant
Preanalytix GmbH
Product code
NTW
Decision date
2009-02-04
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
24150
3005202328
3005202328
PREANALYTIX GMBH
1
N
2026-01-01
Garstligweg 8 HOMBRECHTIKON Zurich CH CH-8634