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
1729801682
Device Listing 1729801682
Listing Summary
#
Listing key
1729801682
Premarket submission
K133983
Device
INTRA. OX HANDHELD TISSUE OXIMETER
Applicant
Vioptix, Inc.
Product code
MUD
Decision date
2014-09-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
60780
3003965364
3003965364
VIOPTIX, INC.
1
N
2026-01-01
39655 Eureka Dr Newark CA US 94560