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

AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081

K Number: K896270 · Decision Dec 12, 1989
Classifications
1
FEI Numbers
49
Registration Numbers
49
Same Product Code
49
Applicant Total
94
Review Days
42

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Basic Information

Device Name
AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
K Number
K896270
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1260
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
October 31, 1989
Decision Date
December 12, 1989
Product Code
CHP
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
CHP Radioimmunoassay, Estradiol

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Other Clearances by Amersham Corp.

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
K904666 AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008
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
K895872 LAN.0800Q/2800Q
Search all 94 clearances from Amersham Corp. →