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
2056083061
Device Listing 2056083061
Listing Summary
#
Listing key
2056083061
Premarket submission
K050352
Device
IN-VITRO DIAGNOSTIC VAGINITIS TEST KIT
Applicant
Ameritek Research, LLC
Product code
JTO
Decision date
2005-09-01
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
12564
3025672
1000126037
AMERITEKUSA, INC.
1
N
2026-01-01
125 130th St SE Ste 200 EVERETT WA US 98208