510(k) K984114
K984114 is an FDA 510(k) premarket notification submitted by Mettler Electronics Corp. for the device "SYS STIM 294, MODEL ME 294". The FDA issued a decision of Substantially Equivalent on February 9, 1999. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Mettler Electronics Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 9, 1999
- Date Received
- November 17, 1998
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Powered
- Device Class
- Class II
- Regulation Number
- 890.5850
- Review Panel
- PM
- Submission Type