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T3 CLASP-BEAD EIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893620
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1989
Days to Decision
92 days

T3 CLASP-BEAD EIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K893620
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/11/1989
Days to Decision
92 days