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

PHENYTOIN RIA KIT

K Number: K770779 · Decision Jun 17, 1977
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
4
Applicant Total
94
Review Days
49

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Basic Information

Device Name
PHENYTOIN RIA KIT
K Number
K770779
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.3350
Medical Specialty
Clinical Toxicology
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
April 29, 1977
Decision Date
June 17, 1977
Product Code
DLP
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
DLP Radioimmunoassay, Diphenylhydantoin

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