510(k) K810466
K810466 is an FDA 510(k) premarket notification submitted by Syva Co. for the device "ETHYL ALCOHOL SERUM CALIBRATOR". The FDA issued a decision of Substantially Equivalent on March 6, 1981. The device falls under product code DNN (Calibrators, Ethyl Alcohol), a Class II device regulated under 21 CFR 862.3200. Syva Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- March 6, 1981
- Date Received
- February 23, 1981
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Calibrators, Ethyl Alcohol
- Device Class
- Class II
- Regulation Number
- 862.3200
- Review Panel
- TX
- Submission Type