510(k) K891169
K891169 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "DADE THROMBOPLASTIN IS". The FDA issued a decision of Substantially Equivalent on Apr 10, 1989. The device falls under product code GJS (Test, Time, Prothrombin), a Class II device regulated under 21 CFR 864.7750. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Apr 10, 1989
- Date Received
- Mar 6, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Test, Time, Prothrombin
- Device Class
- Class II
- Regulation Number
- 864.7750
- Review Panel
- HE
- Submission Type
- 510(k)