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DYNAREX ULTRASOUND GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102637
510(k) Type
Traditional
Applicant
DYNAREX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2011
Days to Decision
155 days
Submission Type
Summary

DYNAREX ULTRASOUND GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K102637
510(k) Type
Traditional
Applicant
DYNAREX CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/16/2011
Days to Decision
155 days
Submission Type
Summary