510(k) K895262

NORMAL COAGULATION CONTROL PLASMA (NCCP) by Medical Diagnostic Technologies, Inc. — Product Code GIZ

K895262 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "NORMAL COAGULATION CONTROL PLASMA (NCCP)". The FDA issued a decision of Substantially Equivalent on October 6, 1989. The device falls under product code GIZ (Plasma, Control, Normal), a Class II device regulated under 21 CFR 864.5425. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 6, 1989
Date Received
August 22, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plasma, Control, Normal
Device Class
Class II
Regulation Number
864.5425
Review Panel
HE
Submission Type