510(k) K781529
K781529 is an FDA 510(k) premarket notification submitted by Xomed, Inc. for the device "SEPTAL BUTTON". The FDA issued a decision of Substantially Equivalent on October 17, 1978. The device falls under product code LFB (Button, Nasal Septal), a Class U device. Xomed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 17, 1978
- Date Received
- September 5, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Button, Nasal Septal
- Device Class
- Class U
- Regulation Number
- Review Panel
- EN
- Submission Type