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
1919199524
Device Listing 1919199524
Listing Summary
#
Listing key
1919199524
Premarket submission
K971111
Device
TRI-TECH INC., EVACUATED BLOOD COLLECTION TUBE, GRAY STOPPER
Applicant
Tri-Tech, Inc.
Product code
JKA
Decision date
1997-06-16
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
101032
1036781
1000111918
TRI-TECH FORENSICS, INC.
1
Y
2026-01-01
3811 International Blvd NE Suite 100 Leland NC US 28451