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ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191240
510(k) Type
Traditional
Applicant
ZEUS Scientific Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2019
Days to Decision
82 days
Submission Type
Statement

ZEUS ELISA Borrelia VlsE1/pepC10 IgG/IgM Test System; ZEUS ELISA Borrelia burgdorferi IgM Test System

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K191240
510(k) Type
Traditional
Applicant
ZEUS Scientific Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2019
Days to Decision
82 days
Submission Type
Statement