510(k) K862497
K862497 is an FDA 510(k) premarket notification submitted by Microtek Medical, Inc. for the device "MICROTEK SEPTAL BUTTON". The FDA issued a decision of Substantially Equivalent on July 14, 1986. The device falls under product code LFB (Button, Nasal Septal), a Class U device. Microtek Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- July 14, 1986
- Date Received
- July 1, 1986
- 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