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MERIFLUOR-CRYPTOSPORIDIUM/GIARDIA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912408
510(k) Type
Traditional
Applicant
MERIDIAN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
54 days
Submission Type
Statement

MERIFLUOR-CRYPTOSPORIDIUM/GIARDIA

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K912408
510(k) Type
Traditional
Applicant
MERIDIAN DIAGNOSTICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/1991
Days to Decision
54 days
Submission Type
Statement