FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

TRICYCLIC ANTIDEPRESSANTS I TX CONTROL

K Number: K800888 · Decision May 2, 1980
Classifications
1
FEI Numbers
43
Registration Numbers
43
Same Product Code
201
Applicant Total
23
Review Days
15

Basic Information

Device Name
TRICYCLIC ANTIDEPRESSANTS I TX CONTROL
K Number
K800888
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
UTAK LABORATORIES, INC.
Date Received
April 17, 1980
Decision Date
May 2, 1980
Product Code
DIF
Advisory Committee
Clinical Toxicology
Review Advisory Committee
TX
Third Party
N

Classifications

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

Product Code Device Name
DIF Drug Mixture Control Materials

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