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

DAC-CEL HCG-MCA KIT RD52

K Number: K831073 · Decision Sep 1, 1983
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
35
Applicant Total
28
Review Days
150

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Basic Information

Device Name
DAC-CEL HCG-MCA KIT RD52
K Number
K831073
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1370
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Applicant
Wellcome Diagnostics
Date Received
April 4, 1983
Decision Date
September 1, 1983
Product Code
CFL
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
CFL Radioimmunoassay, Human Growth Hormone

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K890146 WELLCOLEX COLOUR SALMONELLA TEST ZL 50
K875311 WELLCOZYME HSV WZO2
K861628 WELLCOZYME ROTAVIRUS WZ01
K864206 REVEAL COLOUR STREP A ZL16
K861634 THE WELLCOME ROTAVIRUS LATEX TEST ZL40
K854852 WELLCOGEN BACTERIAL ANTIGEN KIT
K854851 WELLCOGEN N. MENINGITIDIS B/E. COLI K1 ZL24
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