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

GSP INSTRUMENT AND GSP NEONATAL HTSH KIT

K Number: K090846 · Decision Sep 3, 2009
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
17
Review Days
157

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Basic Information

Device Name
GSP INSTRUMENT AND GSP NEONATAL HTSH KIT
K Number
K090846
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Perkinelmer, Inc.
Date Received
March 30, 2009
Decision Date
September 3, 2009
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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