The following data is part of a premarket notification filed by Centers For Disease Control And Prevention with the FDA for Non-variola Orthopoxvirus Real-time Pcr Primer And Probe Set.
Device ID | K221834 |
510k Number | K221834 |
Device Name: | Non-variola Orthopoxvirus Real-time PCR Primer And Probe Set |
Classification | Non-variola Orthopoxvirus Real-time Pcr Primer And Probe Set |
Applicant | Centers For Disease Control And Prevention 1600 Clifton Rd, NE MS H24-11 ATLANTA, GA 30329 |
Contact | Julie Villanueva, PhD |
Correspondent | Julie Villanueva, PhD Centers For Disease Control And Prevention 1600 Clifton Rd, NE MS H24-11 ATLANTA, GA 30329 |
Product Code | PBK |
CFR Regulation Number | 866.3315 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2022-06-23 |
Decision Date | 2022-06-24 |