510(k) K884385

FIBRI-PREST/THROMBIN-PREST CONTROLS by American Bioproducts Co. — Product Code GJA

K884385 is an FDA 510(k) premarket notification submitted by American Bioproducts Co. for the device "FIBRI-PREST/THROMBIN-PREST CONTROLS". The FDA issued a decision of Substantially Equivalent on December 28, 1988. The device falls under product code GJA (Test, Thrombin Time), a Class II device regulated under 21 CFR 864.7875. American Bioproducts Co. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 28, 1988
Date Received
October 18, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Test, Thrombin Time
Device Class
Class II
Regulation Number
864.7875
Review Panel
HE
Submission Type