3M Tegaderm Silver (AG) Mesh
FDA 510(k) K053256 · 3M Company
510(k) numberK053256
Submission
- Device name
- 3M Tegaderm Silver (AG) Mesh
- Applicant
- 3M Company
St. Paul, MN, US - Received
- November 22, 2005
- Decision date
- December 16, 2005
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- FRO – Dressing, Wound, Drug
- Device class
- Unclassified
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Questions and answers
When was 3M Tegaderm Silver (AG) Mesh cleared by the FDA?
3M Tegaderm Silver (AG) Mesh (K053256) received a 510(k) decision of Substantially Equivalent on December 16, 2005, 24 days after the submission was received.
What is the product code of K053256?
The FDA product code is FRO – Dressing, Wound, Drug, a Unclassified device.