510(k) K926567
K926567 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "BAXTER CA DIALYZER". The FDA issued a decision of Substantially Equivalent on Jan 11, 1995. The device falls under product code FJI (Dialyzer, Capillary, Hollow Fiber), a Class II device regulated under 21 CFR 876.5820. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jan 11, 1995
- Date Received
- Dec 31, 1992
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Dialyzer, Capillary, Hollow Fiber
- Device Class
- Class II
- Regulation Number
- 876.5820
- Review Panel
- GU
- Submission Type
- 510(k)