510(k) K121724

ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2 by Richard Wolf Medical Instruments Corp. — Product Code FCW

K121724 is an FDA 510(k) premarket notification submitted by Richard Wolf Medical Instruments Corp. for the device "ENDOLIGHT LED 1.1 ENDOLIGHTLED 1.2". The FDA issued a decision of Substantially Equivalent on September 20, 2012. The device falls under product code FCW (Light Source, Fiberoptic, Routine), a Class II device regulated under 21 CFR 876.1500. Richard Wolf Medical Instruments Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 20, 2012
Date Received
June 12, 2012
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Light Source, Fiberoptic, Routine
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type