FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EMIT LIDOCAINE CONTROL

K Number: K772167 · Decision Nov 22, 1977
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
122
Applicant Total
448
Review Days
6

Basic Information

Device Name
EMIT LIDOCAINE CONTROL
K Number
K772167
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3200
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
SYVA CO.
Date Received
November 16, 1977
Decision Date
November 22, 1977
Product Code
DLJ
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
DLJ Calibrators, Drug Specific

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K011947 EMIT 2000 VALPROIC ACID ASSAY, MODEL OSR4G229UL
K011528 EMIT 2000 PHENOBARBITAL ASSAY, MODEL OSR4D229
K011347 EMIT 2000 PHENYTOIN ASSAY, MODEL 0SR4A229
K993980 SYVA EMIT II PLUS ETHYL ALCOHOL ASSAY, MODELS 9K309UL/9K409UL
K993981 SYVA EMIT II PLUS PROPOXYPHENE ASSAY, MODELS 9G029UL/9G129UL
K993029 ABBOTT AEROSET THEOPHYLLINE ASSAY AND CALIBRATORS; MODELS 1E09 AND 6E89
K993031 ABBOTT AEROSET PHENOBARBITAL ASSEY AND CALIBRATORS;MODELS 1E08 AND 5F54
K993988 SYVA EMIT II PLUS COCAINE METABOLITE ASSAY, MODEL 9H029UL
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