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

VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM

K Number: K022800 · Decision Nov 25, 2002
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
8
Review Days
94

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Basic Information

Device Name
VISIQUANT ANTI-NUCLEAR ANTIBODY TEST SYSTEM
K Number
K022800
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Hyperion, Inc.
Date Received
August 23, 2002
Decision Date
November 25, 2002
Product Code
DHN
Advisory Committee
Immunology
Review Advisory Committee
IM
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
DHN Antinuclear Antibody, Indirect Immunofluorescent, Antigen, Control

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Other Clearances by Hyperion, Inc.

K Number Device Name
K013213 HYPERION VISIQUANT ANA TEST KIT
K935983 MICROREADER 4
K913809 HY-PREP SYSTEM
K873138 MICRO-READER II
K864060 MICRO-READER
K855149 COMPUTING SPECTROPHOTOMETER BIO-CHEMISTRY ANALYZER
K834071 LYMPHANGIOGRAPHY SET SPECIAL 30G