Last synced on 27 January 2023 at 11:04 pm

RESTORELLE L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122440
510(k) Type
Traditional
Applicant
COLOPLAST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2012
Days to Decision
101 days
Submission Type
Summary

RESTORELLE L

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K122440
510(k) Type
Traditional
Applicant
COLOPLAST CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/19/2012
Days to Decision
101 days
Submission Type
Summary