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IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921968
510(k) Type
Traditional
Applicant
TECH-CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
1523 days
Submission Type
Statement

IN VITRO DIAGNOSTIC REAGENT SET, INDIR. PREG. TEST

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K921968
510(k) Type
Traditional
Applicant
TECH-CO, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
6/28/1996
Days to Decision
1523 days
Submission Type
Statement