510(k) K921989
K921989 is an FDA 510(k) premarket notification submitted by Biomerieux Vitek, Inc. for the device "FDP - SLIDEX DIRECT". The FDA issued a decision of Substantially Equivalent on November 3, 1993. The device falls under product code GHH (Fibrin Split Products), a Class II device regulated under 21 CFR 864.7320. Biomerieux Vitek, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 3, 1993
- Date Received
- April 28, 1992
- 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