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

VIRGO(TM) RUBELLA IGG ELISA

K Number: K873088 · Decision Sep 9, 1987
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
93
Applicant Total
41
Review Days
35

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Basic Information

Device Name
VIRGO(TM) RUBELLA IGG ELISA
K Number
K873088
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3510
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Electro-Nucleonics Laboratories, Inc.
Date Received
August 5, 1987
Decision Date
September 9, 1987
Product Code
LFX
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
LFX Enzyme Linked Immunoabsorbent Assay, Rubella

Similar 510(k) Clearances

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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.
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
K853373 DELTA TROL I & II
Search all 41 clearances from Electro-Nucleonics Laboratories, Inc. →