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

AMERLITE REPRODUCTIVE ENDOCRINOLOGY (LABEL CHANGE)

K Number: K890708 · Decision Mar 20, 1989
Classifications
1
FEI Numbers
135
Registration Numbers
135
Same Product Code
672
Applicant Total
94
Review Days
48

Basic Information

Device Name
AMERLITE REPRODUCTIVE ENDOCRINOLOGY (LABEL CHANGE)
K Number
K890708
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
AMERSHAM CORP.
Date Received
January 31, 1989
Decision Date
March 20, 1989
Product Code
JJY
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
JJY Multi-Analyte Controls, All Kinds (Assayed)

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K901832 GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415
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K901848 GADOLINIUM-153 BONE DENSITOMETER SOURCES
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K896270 AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
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