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

THERACHEM ANTI CONVULSANTA THEOPHYLLINE

K Number: K810504 · Decision Mar 11, 1981
Classifications
1
FEI Numbers
41
Registration Numbers
41
Same Product Code
201
Applicant Total
89
Review Days
15

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Basic Information

Device Name
THERACHEM ANTI CONVULSANTA THEOPHYLLINE
K Number
K810504
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.3280
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Fisher Scientific Co., LLC
Date Received
February 24, 1981
Decision Date
March 11, 1981
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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