510(k) K940792
K940792 is an FDA 510(k) premarket notification submitted by Chrono-Log Corp. for the device "AGGRO/LINK VW COFACTOR SOFTWARE". The FDA issued a decision of Substantially Equivalent on Oct 13, 1994. The device falls under product code JOZ (System, Automated Platelet Aggregation), a Class II device regulated under 21 CFR 864.5700. Chrono-Log Corp. has 15 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Oct 13, 1994
- Date Received
- Feb 22, 1994
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- System, Automated Platelet Aggregation
- Device Class
- Class II
- Regulation Number
- 864.5700
- Review Panel
- HE
- Submission Type
- 510(k)