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

AMERLEX-M B-HUMAN CHORIONIC GONADTROPIN RADIOI KIT

K Number: K852675 · Decision Jul 22, 1985
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
374
Applicant Total
94
Review Days
28

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Basic Information

Device Name
AMERLEX-M B-HUMAN CHORIONIC GONADTROPIN RADIOI KIT
K Number
K852675
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
862.1155
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Amersham Corp.
Date Received
June 24, 1985
Decision Date
July 22, 1985
Product Code
JHI
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
JHI Visual, Pregnancy Hcg, Prescription Use

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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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