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Diazyme DZ-Lite iFlash Total beta-hCG Assay, Diazyme DZ-Lite iFlash 1800 Chemiluminescence Immunoassay Analyzer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212221
510(k) Type
Traditional
Applicant
Diazyme Laboratories Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2021
Days to Decision
150 days
Submission Type
Statement

Diazyme DZ-Lite iFlash Total beta-hCG Assay, Diazyme DZ-Lite iFlash 1800 Chemiluminescence Immunoassay Analyzer

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212221
510(k) Type
Traditional
Applicant
Diazyme Laboratories Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/13/2021
Days to Decision
150 days
Submission Type
Statement