Last synced on 23 May 2025 at 11:06 pm

KETTOSIL AND SILGINAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082157
510(k) Type
Traditional
Applicant
KETTENBACH GMBH & CO KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/6/2008
Days to Decision
6 days
Submission Type
Summary

KETTOSIL AND SILGINAT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K082157
510(k) Type
Traditional
Applicant
KETTENBACH GMBH & CO KG
Country
Germany
FDA Decision
Substantially Equivalent
Decision Date
8/6/2008
Days to Decision
6 days
Submission Type
Summary