FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS

K Number: K043072 · Decision Jan 27, 2005
Classifications
1
FEI Numbers
22
Registration Numbers
22
Same Product Code
18
Applicant Total
62
Review Days
80

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Basic Information

Device Name
GEN-PROBE APTIMA ASSAY FOR CHLAMYDIA TRACHOMATIS
K Number
K043072
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.3120
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Gen-Probe, Inc.
Date Received
November 8, 2004
Decision Date
January 27, 2005
Product Code
MKZ
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
MKZ Dna Probe, Nucleic Acid Amplification, Chlamydia

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (MKZ), ordered by most recent decision date.

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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. →