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

VMA BY HPLC TEST (VANILMANDELIC ACID)

K Number: K861010 · Decision May 1, 1986
Classifications
1
FEI Numbers
2
Registration Numbers
2
Same Product Code
11
Applicant Total
319
Review Days
44

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Basic Information

Device Name
VMA BY HPLC TEST (VANILMANDELIC ACID)
K Number
K861010
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1795
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Bio-Rad
Date Received
March 18, 1986
Decision Date
May 1, 1986
Product Code
CDF
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

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

Product Code Device Name
CDF Acid, Vanilmandelic, Diazo, P-Nitroaniline/Vanillin

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