510(k) K902976
K902976 is an FDA 510(k) premarket notification submitted by Medical Consultants Intl. , Ltd. for the device "MEDI MODEL SBL502-B (LISS BODY STIMULATOR) ZERO DC". The FDA issued a decision of Substantially Equivalent on September 7, 1990. The device falls under product code GZL (Electrode, Depth), a Class II device regulated under 21 CFR 882.1330. Medical Consultants Intl. , Ltd. has at least 5 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 7, 1990
- Date Received
- July 6, 1990
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Electrode, Depth
- Device Class
- Class II
- Regulation Number
- 882.1330
- Review Panel
- NE
- Submission Type