510(k) K863594
K863594 is an FDA 510(k) premarket notification submitted by American Dade for the device "ACTIN FSL ACTIVATED PTT REAGENT". The FDA issued a decision of Substantially Equivalent on October 17, 1986. The device falls under product code GGW (Test, Time, Partial Thromboplastin), a Class II device regulated under 21 CFR 864.7925. American Dade has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- October 17, 1986
- Date Received
- September 15, 1986
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Test, Time, Partial Thromboplastin
- Device Class
- Class II
- Regulation Number
- 864.7925
- Review Panel
- HE
- Submission Type