510(k) K853113

Device
Td Tricyclic Antidepressants
Applicant
ABBOTT LABORATORIES
510(k) number
K853113
Product code
LFG
Decision
Substantially Equivalent (SESE)
Decision date
1985-08-12
Date received
1985-07-24
Regulation
862.3910
Classification name
Radioimmunoassay, Tricyclic Antidepressant Drugs
Medical specialty
Clinical Toxicology
Review panel
Clinical Toxicology
Device class
2
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Contact
MARY E ZORC
Address
One Abbott Park Rd. Abbott Park IL US 60064 60064

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

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