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

VIRGO REAGENTS INDIRECT FLUORSCENT

K Number: K841127 · Decision Apr 25, 1984
Classifications
1
FEI Numbers
21
Registration Numbers
21
Same Product Code
109
Applicant Total
41
Review Days
40

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Basic Information

Device Name
VIRGO REAGENTS INDIRECT FLUORSCENT
K Number
K841127
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.5100
Medical Specialty
Immunology
Decision
Substantially Equivalent
Applicant
Electro-Nucleonics Laboratories, Inc.
Date Received
March 16, 1984
Decision Date
April 25, 1984
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 Electro-Nucleonics Laboratories, Inc.

K Number Device Name
K873925 VIRGO(TM) MEASLES IGG ELISA
K873617 GEMSTAR II SYSTEM
K873416 MULTI-ACCESS REAGENT DISPENSER
K873358 GEMENI URIC ACID U.V.
K873088 VIRGO(TM) RUBELLA IGG ELISA
K871905 TOXOPLASMA GONDII IGG ELISA
K870928 CHOLESTEROL (TOTAL) ANALYSIS PRODUCTS
K863874 LIPASE HYDROLYSIS/GLYCEROL KINASE, TRIGLYCERIDES
K862640 AMYLASE LTS
K853372 GEMSTAR IPA THEOPHYLLINE TEST KIT
Search all 41 clearances from Electro-Nucleonics Laboratories, Inc. →