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OPTICOAT T3 EIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981824
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
214 days
Submission Type
Statement

OPTICOAT T3 EIA KIT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K981824
510(k) Type
Traditional
Applicant
BIOTECX LABORATORIES, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/22/1998
Days to Decision
214 days
Submission Type
Statement