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
1991834542
Device Listing 1991834542
Listing Summary
#
Listing key
1991834542
Premarket submission
K093259
Device
ARP RX100
Applicant
Arp Manufacturing, Inc.
Product code
IPF
Decision date
2009-12-17
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
33109
1721868
3001237153
ARP Manufacturing, LLC
1
N
2020-04-25
7270 S Fraser St Centennial CO US 80112