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

MODIFIED TOXOPLASMA GONDII IGG EIA TEST KIT

K Number: K872252 · Decision Jul 1, 1987
Classifications
1
FEI Numbers
36
Registration Numbers
36
Same Product Code
105
Applicant Total
16
Review Days
20

Basic Information

Device Name
MODIFIED TOXOPLASMA GONDII IGG EIA TEST KIT
K Number
K872252
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3780
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
LABSYSTEMS, INC.
Date Received
June 11, 1987
Decision Date
July 1, 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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LGD), ordered by most recent decision date.

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Other Clearances by LABSYSTEMS, INC.

K Number Device Name
K896474 RESUBMITTED FECATWIN SENSITIVE - FECA-EIA
K890154 MODIFIED LABYSYSTEMS' TOXOPLASMA GONDII IGG EIA
K890091 MODIFIED LABSYSTEMS' RUBELLA IGG EIA TEST KIT
K881243 RUBELLA IGG - EIA TEST KIT NUMBER 61 07 201
K873780 MODIFICATION RUBELLA IGM EIA TEST KIT
K873583 AUTO-EIA
K862705 CYTOMEGALOVIRUS IGG EIA TEST KIT
K862431 RUBELLA IGM EIA TEST KIT
K862216 TOXOPLASMA GONDII IGG EIA TEST KIT (AMENDMENT)
K853696 RUBELLA IGG EIA TEST KIT
Search all 16 clearances from LABSYSTEMS, INC. →