510(k) K983628

XENON LIGHT SOURCE AUTO LIP 5123, MODEL 2123.011 by Richard Wolf Medical Instruments Corp. — Product Code GCT

K983628 is an FDA 510(k) premarket notification submitted by Richard Wolf Medical Instruments Corp. for the device "XENON LIGHT SOURCE AUTO LIP 5123, MODEL 2123.011". The FDA issued a decision of Substantially Equivalent on December 11, 1998. The device falls under product code GCT (Light Source, Endoscope, Xenon Arc), 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
December 11, 1998
Date Received
October 15, 1998
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Light Source, Endoscope, Xenon Arc
Device Class
Class II
Regulation Number
876.1500
Review Panel
GU
Submission Type