510(k) K823865
K823865 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "ADVANCE SYS. EMIT-CAD LIDOCAINE CONTROL". The FDA issued a decision of Substantially Equivalent on January 14, 1983. The device falls under product code LAX (Lidocaine Control Materials), a Class I device regulated under 21 CFR 862.3280. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 14, 1983
- Date Received
- December 23, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Lidocaine Control Materials
- Device Class
- Class I
- Regulation Number
- 862.3280
- Review Panel
- TX
- Submission Type