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

Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer

K Number: K221225 · Decision Nov 10, 2022
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
270
Review Days
196

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Basic Information

Device Name
Access TSH (3rd IS) Assay, DxI 9000 Access Immunoassay Analyzer
K Number
K221225
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Beckman Coulter, Inc.
Date Received
April 28, 2022
Decision Date
November 10, 2022
Product Code
JLW
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
JLW Radioimmunoassay, Thyroid-Stimulating Hormone

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