510(k) K841021

HEMOTEC, HEPCON/SYS B-10 HEPARIN/PROTAM by Hemotec, Inc. — Product Code JOX

K841021 is an FDA 510(k) premarket notification submitted by Hemotec, Inc. for the device "HEMOTEC, HEPCON/SYS B-10 HEPARIN/PROTAM". The FDA issued a decision of Substantially Equivalent on May 25, 1984. The device falls under product code JOX (Analyzer, Heparin, Automated), a Class II device regulated under 21 CFR 864.5680. Hemotec, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 25, 1984
Date Received
March 12, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Analyzer, Heparin, Automated
Device Class
Class II
Regulation Number
864.5680
Review Panel
HE
Submission Type