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
1696382194
Device Listing 1696382194
Listing Summary
#
Listing key
1696382194
Premarket submission
K052435
Device
PNEUMRX FAMILY OF BIOPSY NEEDLES AND KITS
Applicant
Pneumrx, Inc.
Product code
KNW
Decision date
2005-11-03
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
233907
3001627457
3001627457
EKOS Corporation
1
Y
2020-04-25
11911 N. Creek Parkway South Bothell WA US 98011