510(k) K890399
K890399 is an FDA 510(k) premarket notification submitted by American Bioproducts Co. for the device "MODIFIED D-DI-TEST KIT". The FDA issued a decision of Substantially Equivalent on February 7, 1989. The device falls under product code GHH (Fibrin Split Products), a Class II device regulated under 21 CFR 864.7320. American Bioproducts Co. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- February 7, 1989
- Date Received
- January 24, 1989
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Fibrin Split Products
- Device Class
- Class II
- Regulation Number
- 864.7320
- Review Panel
- HE
- Submission Type