Last synced on 25 January 2026 at 3:41 am

TYTRON C-500IR CLINICAL INFRARED IMAGING SYSTEM

Page Type
Cleared 510(K)
PDF
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
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