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REGUTHERM 952 THERMOGRAPHIC SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003130
510(k) Type
Traditional
Applicant
SIE-MED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2001
Days to Decision
133 days
Submission Type
Summary

REGUTHERM 952 THERMOGRAPHIC SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K003130
510(k) Type
Traditional
Applicant
SIE-MED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2001
Days to Decision
133 days
Submission Type
Summary