510(k) K921989

FDP - SLIDEX DIRECT by Biomerieux Vitek, Inc. — Product Code GHH

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