Atlas FDA

MERITEC(TM) - C. DIFFICILE LATEX TEST SYSTEM

FDA 510(k) clearance K895915 · decided 1990-03-12

Clearance details

K-number
K895915
Device name
MERITEC(TM) - C. DIFFICILE LATEX TEST SYSTEM
Applicant
Meridian Diagnostics, Inc.
Decision
Substantially Equivalent
Date received
1989-10-10
Decision date
1990-03-12
Days to decision
153 days
Clearance type
Traditional
Product code
MCB
Device class
1
Regulation number
866.2660
Medical specialty
Microbiology
Advisory committee
Microbiology
Location
Cincinnati, OH, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
VIDAS C DIFFICILE GDH (K132010)Biomerieux S.A.2013-10-09
IMMUNOCARD C. DIFFICILE GDH (K112048)Meridian Bioscience, Inc.2011-12-16
PREMIER C. DIFFICILE GDH (K110620)Meridian Bioscience, Inc.2011-05-03
C. DIFF QUIK CHEK (K053572)Techlab, Inc.2006-04-26
TRIAGE C. DIFFICILE, TRIAGE C. DIFFICILE PANEL, TRIAGE C. DIFFICILE TOXIN A (K974881)Biosite Incorporated1998-03-20
CLEARVIEW C. DIFF A (K955067)Unipath , Ltd.1996-09-13
MERITEC C. DIFFICILE CONTROLS (K924062)Meridian Diagnostics, Inc.1992-10-19
CLOSTRIDIUM DIFFICILE TOXIN A ENZYME IMMUNOASSAY (K904329)Baxter Healthcare Corp1991-03-12
CYTOTOXICITY ASSAY FOR CLOSTRIDIUM- (K833447)Bartels Immunodiagnostic Supplies, Inc.1984-05-21

Recalls involving this device

No recalls on record reference this clearance.