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
1517251615
Device Listing 1517251615
Listing Summary
#
Listing key
1517251615
Premarket submission
K140367
Device
ARCHITECT PX EXTRACELLULAR COLLAGEN MATRIX
Applicant
Harbor Medtech, Inc.
Product code
KGN
Decision date
2014-09-12
Related Registrations
#
Registration key, Registration, FEI table
Registration key
Registration
FEI
Company
Status
Initial importer
Expiration
Address
328957
3010097129
3010097129
HARBOR MEDTECH, INC.
1
N
2026-01-01
21076 Bake Parkway Suite 100 Lake Forest CA US 92630