510(k) K092593
K092593 is an FDA 510(k) premarket notification submitted by Atos Medical AB for the device "PROVOX ACTIVALVE (SIZE 4.5MM, 6MM, 8MM, 10MM, 12.5MM)". The FDA issued a decision of Substantially Equivalent (kit) on October 14, 2010. The device falls under product code EWL (Prosthesis, Laryngeal (Taub)), a Class II device regulated under 21 CFR 874.3730. Atos Medical AB has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESK (Substantially Equivalent (kit))
- Decision Date
- October 14, 2010
- Date Received
- August 24, 2009
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Laryngeal (Taub)
- Device Class
- Class II
- Regulation Number
- 874.3730
- Review Panel
- EN
- Submission Type