510(k) K792713

CANDIDA ALBICANS, ANTISERUM by Meridian Diagnostics, Inc. — Product Code GMI

K792713 is an FDA 510(k) premarket notification submitted by Meridian Diagnostics, Inc. for the device "CANDIDA ALBICANS, ANTISERUM". The FDA issued a decision of Substantially Equivalent on January 23, 1980. The device falls under product code GMI (Antigen, Cf And / Or Id, Coccidioides Immitis), a Class II device regulated under 21 CFR 866.3135. Meridian Diagnostics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 23, 1980
Date Received
December 27, 1979
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Antigen, Cf And / Or Id, Coccidioides Immitis
Device Class
Class II
Regulation Number
866.3135
Review Panel
MI
Submission Type