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KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130377
510(k) Type
Special
Applicant
MEDICATECH USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2013
Days to Decision
92 days
Submission Type
Summary

KRYSTALRAD NEW SERIESDIGITAL RADIOGRAPHIC PORTABLE RETROFIT SYSTEM

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K130377
510(k) Type
Special
Applicant
MEDICATECH USA
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/17/2013
Days to Decision
92 days
Submission Type
Summary