510(k) K780632
K780632 is an FDA 510(k) premarket notification submitted by Med General for the device "MAXICEPTOR". The FDA issued a decision of Substantially Equivalent on August 14, 1978. The device falls under product code ISB (Stimulator, Muscle, Diagnostic), a Class II device regulated under 21 CFR 890.1850. Med General has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 14, 1978
- Date Received
- April 17, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Stimulator, Muscle, Diagnostic
- Device Class
- Class II
- Regulation Number
- 890.1850
- Review Panel
- PM
- Submission Type