510(k) K032598
K032598 is an FDA 510(k) premarket notification submitted by Synergetics, Inc. for the device "SYNERGETICS SYNERLIGHT FIBER OPTIC LIGHTSOURCE". The FDA issued a decision of Substantially Equivalent on November 24, 2003. The device falls under product code MPA (Endoilluminator), a Class II device regulated under 21 CFR 876.1500. Synergetics, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 24, 2003
- Date Received
- August 25, 2003
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Endoilluminator
- Device Class
- Class II
- Regulation Number
- 876.1500
- Review Panel
- OP
- Submission Type