FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

MEASELISA TEST KIT

K Number: K821762 · Decision Jul 30, 1982
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
10
Applicant Total
12
Review Days
45

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Basic Information

Device Name
MEASELISA TEST KIT
K Number
K821762
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3520
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
M.A. Bioproducts
Date Received
June 15, 1982
Decision Date
July 30, 1982
Product Code
LJB
Advisory Committee
Microbiology
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
LJB Enzyme Linked Immunoabsorbent Assay, Rubeola Igg

Similar 510(k) Clearances

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

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Other Clearances by M.A. Bioproducts

K Number Device Name
K822883 HERPELISA KIT
K823804 MYCOPLASMELISA TEST KIT
K830045 MUMPSELISA TEST KIT
K830615 CYTOMEGELISA STAT
K823805 VARICELISA TEST KIT
K821967 CHLAMYDELISA TEST KIT
K813221 TOXOELISA TEST KIT
K812531 CELL CULTURE REAGENTS
K812123 CYTOMEGELISA TEST KIT
K802508 RUBELISA IGM TEST KIT
Search all 12 clearances from M.A. Bioproducts →