510(k) K854077
K854077 is an FDA 510(k) premarket notification submitted by Stryker Corp. for the device "MIX EVAC II". The FDA issued a decision of SN on January 31, 1986. The device falls under product code JDZ (Mixer, Cement, For Clinical Use), a Class I device regulated under 21 CFR 888.4210. Stryker Corp. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SN ()
- Decision Date
- January 31, 1986
- Date Received
- October 7, 1985
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mixer, Cement, For Clinical Use
- Device Class
- Class I
- Regulation Number
- 888.4210
- Review Panel
- OR
- Submission Type