510(k) K781302
K781302 is an FDA 510(k) premarket notification submitted by Spembly Medical , Ltd. for the device "NEUROSTAT, LLOYD". The FDA issued a decision of Substantially Equivalent on August 15, 1978. The device falls under product code GXH (Device, Surgical, Cryogenic), a Class II device regulated under 21 CFR 882.4250. Spembly Medical , Ltd. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- August 15, 1978
- Date Received
- July 28, 1978
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Device, Surgical, Cryogenic
- Device Class
- Class II
- Regulation Number
- 882.4250
- Review Panel
- NE
- Submission Type