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TRI-POINT LIQUIMMUNE LIQUID ASSAYED CONTROL LEVELS 1,2, AND 3

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011731
510(k) Type
Traditional
Applicant
Medical Analysis Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2001
Days to Decision
30 days
Submission Type
Statement

TRI-POINT LIQUIMMUNE LIQUID ASSAYED CONTROL LEVELS 1,2, AND 3

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K011731
510(k) Type
Traditional
Applicant
Medical Analysis Systems, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/5/2001
Days to Decision
30 days
Submission Type
Statement