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IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914171
510(k) Type
Traditional
Applicant
TECH INTL. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
92 days
Submission Type
Statement

IN VITRO DIAGNOSTIC REGEANT SET,CHOLINESTERASE

Page Type
Cleared 510(K)
PDF
PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K914171
510(k) Type
Traditional
Applicant
TECH INTL. CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/1991
Days to Decision
92 days
Submission Type
Statement