510(k) K862497

MICROTEK SEPTAL BUTTON by Microtek Medical, Inc. — Product Code LFB

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