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
1343071083
Device Listing 1343071083
Listing Summary
#
Listing key
1343071083
Premarket submission
K941579
Device
MODIFIED MICRO TEST MULTI MICROBE MEDIUM (M5)
Applicant
Microtest
Product code
JSM
Decision date
1994-10-21
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
7644
1924669
1924669
REMEL, INC.
1
Y
2026-01-01
12076 Santa Fe Trail Dr LENEXA KS US 66215