510(k) K875238
K875238 is an FDA 510(k) premarket notification submitted by Elmed, Inc. for the device "SIEMENS NEUROTON 826 AND 827". The FDA issued a decision of Substantially Equivalent on March 10, 1988. The device falls under product code IPF (Stimulator, Muscle, Powered), a Class II device regulated under 21 CFR 890.5850. Elmed, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 10, 1988
- Date Received
- December 22, 1987
- 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