PBK · Class II · 21 CFR 866.3315

Non-variola Orthopoxvirus Real-time Pcr Primer And Probe Set — FDA 510(k) Devices

In Vitro Qualitative Detection Of Non-variola Orthopoxvirus Nucleic Acids Extracted From Human Specimens Or Viral Culture.

3
Total
3
Cleared
3d
Avg days
2022
Since

List of Non-variola Orthopoxvirus Real-time Pcr Primer And Probe Set devices cleared through 510(k)

3 devices
1–3 of 3

How to use this database

This page lists all FDA 510(k) submissions for Non-variola Orthopoxvirus Real-time Pcr Primer And Probe Set devices (product code PBK). Click any device to view full submission details, including the decision date, manufacturer information, predicate device, and a link to the official FDA record.

These devices fall under the Microbiology FDA review panel. Browse all Microbiology devices →