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

TOXICOLOGY CONTROL

K Number: K810201 · Decision Feb 4, 1981
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
82
Applicant Total
23
Review Days
12

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Basic Information

Device Name
TOXICOLOGY CONTROL
K Number
K810201
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
January 23, 1981
Decision Date
February 4, 1981
Product Code
LAS
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
LAS Drug Specific Control Materials

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Other Clearances by Utak Laboratories, Inc.

K Number Device Name
K903061 UTAK LABORATORIES TOXICOLOGY CONTROL
K883147 TRACE ELEMENTS SERUM TOXICOLOGY CONTROL
K862418 BENZODIAZEPINES TOXICOLOGY CONTROL
K862419 SERUM VANCOMYCIN TOXICOLOGY CONTROL
K862421 SERUM CLONAZEPAM TOXICOLOGY CONTROL
K862420 UTAK-STABBS TOXICOLOGY CONTROL
K831736 TRICYCLIC ANTIDEPRESSANTS
K831738 CAFFINE TOXICOLOGY CONTROL
K831735 MAPROTILINE
K831741 FLURAZEPAM TOXICOLOGY CONTROL
Search all 23 clearances from Utak Laboratories, Inc. →