510(k) K890409
K890409 is an FDA 510(k) premarket notification submitted by Baxter Healthcare Corp for the device "DADE(R) PLASMINOGEN CHROMOGENIC ASSAY". The FDA issued a decision of Substantially Equivalent on Feb 27, 1989. The device falls under product code GGP (Test, Qualitative And Quantitative Factor Deficiency), a Class II device regulated under 21 CFR 864.7290. Baxter Healthcare Corp has 507 other 510(k) clearances on record.
Clearance details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Feb 27, 1989
- Date Received
- Jan 24, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device classification
- Device Name
- Test, Qualitative And Quantitative Factor Deficiency
- Device Class
- Class II
- Regulation Number
- 864.7290
- Review Panel
- HE
- Submission Type
- 510(k)