Last synced on 19 July 2024 at 11:05 pm

ULTRAPRO MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033337
510(k) Type
Traditional
Applicant
ETHICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2004
Days to Decision
167 days
Submission Type
Summary

ULTRAPRO MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K033337
510(k) Type
Traditional
Applicant
ETHICON, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/1/2004
Days to Decision
167 days
Submission Type
Summary