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

LYME DISEASE IGM ELISA

K Number: K900206 · Decision Jun 28, 1991
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
110
Applicant Total
33
Review Days
528

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Basic Information

Device Name
LYME DISEASE IGM ELISA
K Number
K900206
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Hillcrest Biologicals
Date Received
January 16, 1990
Decision Date
June 28, 1991
Product Code
LSR
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
LSR Reagent, Borrelia Serological Reagent

Similar 510(k) Clearances

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Other Clearances by Hillcrest Biologicals

K Number Device Name
K913618 ARBOVIRUS IGM IFA TEST
K913617 ARBOVIRUS IGG IFA TEST
K913906 Q FEVER IGG IFA TEST
K922374 Q FEVER IGM IFA TEST
K896594 EBV VCA ANTIBODY (IGM)
K884829 EBV EARLY ANTIGEN (R+D)
K883767 LYME DISEASE IFA (IGM)
K884591 EBV-VCA ANTIBODY (IGG)
K883487 LYME DISEASE IFA (IGG)
K875170 EBNA ANTIBODY
Search all 33 clearances from Hillcrest Biologicals →