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

LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGM (WB0400M)

K Number: K971007 · Decision Jun 1, 1998
Classifications
1
FEI Numbers
30
Registration Numbers
30
Same Product Code
110
Applicant Total
7
Review Days
439

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Basic Information

Device Name
LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGM (WB0400M)
K Number
K971007
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3830
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mrl Diagnostics
Date Received
March 19, 1997
Decision Date
June 1, 1998
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

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Other Clearances by Mrl Diagnostics

K Number Device Name
K000238 HSV-1 & HSV-2 DIFFERENTIATION IMMUNOBLOT IGG, MODEL IB0900G
K993754 HSV-1 ELISA IGG, MODEL EL0910G
K993724 HSV-2 ELISA IGG, MODEL EL0920G
K971006 LYME DISEASE B. BURGDORFERI GENOGROUP 1 WESTERN BLOT IGG (WB0400G)
K946353 EPSTEIN-BARR VIRUS NUCLEAR ANTIGEN RECOMBINANT IMMUNOFLUORESCENT ASSAY
K931520 EPSTEIN-BARR VIRUS VCA (IGM) RECOMB IMMUN ANTIBODY