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

MODIFIED AMERLEX-M PROGESTERONE RADIOIMMUNO. KIT

K Number: K880934 · Decision Apr 18, 1988
Classifications
1
FEI Numbers
47
Registration Numbers
47
Same Product Code
56
Applicant Total
94
Review Days
42

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Basic Information

Device Name
MODIFIED AMERLEX-M PROGESTERONE RADIOIMMUNO. KIT
K Number
K880934
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1620
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
March 7, 1988
Decision Date
April 18, 1988
Product Code
JLS
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
JLS Radioimmunoassay, Progesterone

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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
K896270 AMERLITE ESTRADIOL-60 ASSAY LAN.0081/2081
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