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

VALIDATE THYROID CALIBRATION VERIFICATION / LINEARITY TEST SET, MODEL 901

K Number: K062501 · Decision Sep 29, 2006
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
23
Review Days
35

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Basic Information

Device Name
VALIDATE THYROID CALIBRATION VERIFICATION / LINEARITY TEST SET, MODEL 901
K Number
K062501
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Maine Standards Co.
Date Received
August 25, 2006
Decision Date
September 29, 2006
Product Code
JJX
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
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

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K083891 VALIDATE THYROID CALIBRATION VERIFICATION TEST SET, MODEL 901
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K072246 VALIDATE SP1 CALIBRATION VERIFICATION/LINEARITY TEST SET, MODEL 601
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