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

TOXOPLASMA GONDII IGG ELISA

K Number: K871905 · Decision Jul 30, 1987
Classifications
1
FEI Numbers
32
Registration Numbers
32
Same Product Code
105
Applicant Total
41
Review Days
76

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Basic Information

Device Name
TOXOPLASMA GONDII IGG ELISA
K Number
K871905
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Electro-Nucleonics Laboratories, Inc.
Date Received
May 15, 1987
Decision Date
July 30, 1987
Product Code
LGD
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
LGD Enzyme Linked Immunoabsorbent Assay, Toxoplasma Gondii

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Other Clearances by Electro-Nucleonics Laboratories, Inc.

K Number Device Name
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K873416 MULTI-ACCESS REAGENT DISPENSER
K873358 GEMENI URIC ACID U.V.
K873088 VIRGO(TM) RUBELLA 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. →