Last synced on 27 January 2023 at 11:04 pm

UGYTEX SUAL KNIT MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051503
510(k) Type
Traditional
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
59 days
Submission Type
Summary

UGYTEX SUAL KNIT MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K051503
510(k) Type
Traditional
Applicant
SOFRADIM PRODUCTION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/5/2005
Days to Decision
59 days
Submission Type
Summary