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

AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008

K Number: K904666 · Decision Nov 2, 1990
Classifications
1
FEI Numbers
73
Registration Numbers
73
Same Product Code
241
Applicant Total
94
Review Days
18

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Basic Information

Device Name
AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008
K Number
K904666
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1690
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
October 15, 1990
Decision Date
November 2, 1990
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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K Number Device Name
K914135 AMERLITE(TM) PROLACTIN-30 ASSAY, LAN.0086/2086
K912733 AMERLEX-M SPECIFIC ESTROL(UNCONJUGATED) RIA KIT
K912766 AMERLITE CK-MB ASSAY
K902760 AMERSHAM TSH CONTROL SERA
K901854 GADOLINIUM-153 BONE DENSITOMETER (GDC.10411/10412)
K901857 GADOLINIUM-153 BONE DENSITOMETER (GDC.10413)
K901848 GADOLINIUM-153 BONE DENSITOMETER SOURCES
K901832 GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415
K896270 AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
K895872 LAN.0800Q/2800Q
Search all 94 clearances from Amersham Corp. →