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
1239091507
Device Listing 1239091507
Listing Summary
#
Listing key
1239091507
Premarket submission
K053286
Device
MODIFICATION TO: NXSTAGE PUREFLOW-B SOLUTION
Applicant
Nxstage Medical, Inc.
Product code
KPO
Decision date
2005-12-22
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
233341
3003464075
3003464075
NXSTAGE MEDICAL, INC.
1
N
2026-01-01
350 Merrimack St LAWRENCE MA US 01843