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THYRETAIN TM TSI REPORTER BIOASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092229
510(k) Type
Traditional
Applicant
DIAGNOSTIC HYBRIDS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2010
Days to Decision
299 days
Submission Type
Summary

THYRETAIN TM TSI REPORTER BIOASSAY

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K092229
510(k) Type
Traditional
Applicant
DIAGNOSTIC HYBRIDS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2010
Days to Decision
299 days
Submission Type
Summary