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FDA PRODUCT CODE · CLASS II

PZMNext Generation Sequencing Based Tumor Profiling Test

A next-generation sequencing based tumor profiling test is a qualitative in vitro diagnostic test intended to detect mutations in a broad panel of targeted genes that are somatically altered in malignant neoplasms from tumor specimens obtained from patients diagnosed with malignant solid neoplasms using targeted next-generation sequencing.

DEVICE CLASS
Class II
REGULATION
21 CFR 866.6080
MEDICAL SPECIALTY
Pathology
REVIEW PANEL
PA
ImplantLife-sustainingGMP-exemptThird-party review eligible
3
510(K)/PMA CLEARANCES
510k: 3
0
RECALL ENTRIES

Recent clearances

K260235Datar Cancer Genetics Private Limited · 510k2026-05-12
K241868Tempus AI, Inc. · 510k2025-09-19
K250003Geneseeq Technology, Inc. · 510k2025-08-29

Related on SPEQ

Medical devices industryMedical device quality (ISO 13485)FDA device clearancesFDA enforcement & recalls

Source: FDA device classification, 510(k)/PMA, and recall datasets (openFDA). Recall entries count distinct FDA recall numbers, so one recall event affecting several products appears as several entries. SPEQ is not affiliated with the FDA; this is a reference view of public FDA data.

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