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TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032471
510(k) Type
Traditional
Applicant
TITRONICS RESEARCH & DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2003
Days to Decision
60 days
Submission Type
Summary

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K032471
510(k) Type
Traditional
Applicant
TITRONICS RESEARCH & DEVELOPMENT CO.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/10/2003
Days to Decision
60 days
Submission Type
Summary