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

ARGINIE BROTH

K Number: K842297 · Decision Jun 22, 1984
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
86
Applicant Total
137
Review Days
11

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Basic Information

Device Name
ARGINIE BROTH
K Number
K842297
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Remel Co.
Date Received
June 11, 1984
Decision Date
June 22, 1984
Product Code
JSF
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JSF Culture Media, Single Biochemical Test

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