510(k) K983628
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