FDA 510(k) FDA unclassified Substantially Equivalent 🇺🇸 United States

TDX METHOTREXATE

K Number: K830398 · Decision Mar 10, 1983
Classifications
1
FEI Numbers
4
Registration Numbers
4
Same Product Code
9
Applicant Total
883
Review Days
31

Basic Information

Device Name
TDX METHOTREXATE
K Number
K830398
Device Class
FDA unclassified
Clearance Type
Traditional
Medical Specialty
Unknown
Decision
Substantially Equivalent
Applicant
Abbott Laboratories
Date Received
February 7, 1983
Decision Date
March 10, 1983
Product Code
LAO
Advisory Committee
Unknown
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LAO Enzyme Immunoassay, Methotrexate

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LAO), ordered by most recent decision date.

View all

Other Clearances by Abbott Laboratories

K Number Device Name
K252424 Anti-HCV Next
K243500 ARCHITECT iGentamicin
K243168 Alinity i Rubella IgG
K243283 Alinity h-series System
K233932 Alinity i Toxo IgM
K232669 TBI
K222850 HAVAb IgG II
K220031 Alinity h-series System
K220282 i-STAT PTplus Cartridge with the i-STAT 1 System
K230937 Alinity i Total ß-hCG Reagent Kit, GLP systems Track
Search all 883 clearances from Abbott Laboratories →