510(k) K943468
K943468 is an FDA 510(k) premarket notification submitted by Elekta Instruments, Inc. for the device "LEKSELL SURGIPLAN". The FDA issued a decision of Substantially Equivalent on January 20, 1995. The device falls under product code HAW (Neurological Stereotaxic Instrument), a Class II device regulated under 21 CFR 882.4560. Elekta Instruments, Inc. has at least 7 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 20, 1995
- Date Received
- July 19, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Neurological Stereotaxic Instrument
- Device Class
- Class II
- Regulation Number
- 882.4560
- Review Panel
- NE
- Submission Type