510(k) K873114

CYTOMEGALOVIRUS CONTROL SLIDES by Medical Diagnostic Technologies, Inc. — Product Code GQH

K873114 is an FDA 510(k) premarket notification submitted by Medical Diagnostic Technologies, Inc. for the device "CYTOMEGALOVIRUS CONTROL SLIDES". The FDA issued a decision of Substantially Equivalent on September 25, 1987. The device falls under product code GQH (Antigen, Cf (Including Cf Control), Cytomegalovirus), a Class II device regulated under 21 CFR 866.3175. Medical Diagnostic Technologies, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 25, 1987
Date Received
August 10, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Cf (Including Cf Control), Cytomegalovirus
Device Class
Class II
Regulation Number
866.3175
Review Panel
MI
Submission Type