510(k) K894052

ELECTRA 1000C AUTOMATIC COAGULATION TIMER by Medical Laboratory Automation Systems, Inc. — Product Code GKP

K894052 is an FDA 510(k) premarket notification submitted by Medical Laboratory Automation Systems, Inc. for the device "ELECTRA 1000C AUTOMATIC COAGULATION TIMER". The FDA issued a decision of Substantially Equivalent on July 27, 1989. The device falls under product code GKP (Instrument, Coagulation, Automated), a Class II device regulated under 21 CFR 864.5400. Medical Laboratory Automation Systems, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
July 27, 1989
Date Received
June 7, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Instrument, Coagulation, Automated
Device Class
Class II
Regulation Number
864.5400
Review Panel
HE
Submission Type