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ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931907
510(k) Type
Traditional
Applicant
ANTHOS LABTEC INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1993
Days to Decision
167 days
Submission Type
Summary

ANTHOS HT READERS, INCLUDING THE ANTHOS HT II&III

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K931907
510(k) Type
Traditional
Applicant
ANTHOS LABTEC INSTRUMENTS
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/29/1993
Days to Decision
167 days
Submission Type
Summary