FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ACCUPROBE HISTOPLASMA CAPSULATUM CULTURE CONF.TEST

K Number: K896859 · Decision Feb 1, 1990
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
0
Applicant Total
62
Review Days
58

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Basic Information

Device Name
ACCUPROBE HISTOPLASMA CAPSULATUM CULTURE CONF.TEST
K Number
K896859
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
866.3320
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Gen-Probe, Inc.
Date Received
December 5, 1989
Decision Date
February 1, 1990
Product Code
MBT
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MBT Dna-Probe, Reagent, Histoplasma Capsulatum

Other Clearances by Gen-Probe, Inc.

K Number Device Name
K122062 APTIMA TRICHOMONAS VAGINALIS ASSAY - PANTHER
K111409 APTIMA COMBO 2 ASSAY
K063664 GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE MODEL#1091
K063451 GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1199
K062440 GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1091
K061413 APTIMA CT ASSAY ON THE TIGRIS DTS SYSTEM
K061509 TIGRIS DTS GEN-PROBE APTIMA ASSAY FOR NEISSERIA GONORRHOEAE, MODEL 1196
K060652 TIGRIS DTS GEN-PROBE APTIMA COMBO 2 ASSAY
K053446 GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS, MODEL 1088
K043224 GEN-PROBE APTIMA COMBO 2 ASSAY
Search all 62 clearances from Gen-Probe, Inc. →