510(k) K890399

MODIFIED D-DI-TEST KIT by American Bioproducts Co. — Product Code GHH

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