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UNI-PATCH ULTRASOUND COUPLING GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021132
510(k) Type
Traditional
Applicant
THE LUDLOW COMPANY LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2002
Days to Decision
36 days
Submission Type
Summary

UNI-PATCH ULTRASOUND COUPLING GEL

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K021132
510(k) Type
Traditional
Applicant
THE LUDLOW COMPANY LP
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/15/2002
Days to Decision
36 days
Submission Type
Summary