# PTF: Assay To Measure Pct To Aid In The Risk Assessment Of Critically Ill Patients On Their First Day Of Icu Admission

- Device class: 2; regulation: 21 CFR 866.3215; FDA's rule: 510(k) required
- FDA decisions: 4
- 510(k) review time 2021–2025: median 245 days (middle half 228–263)
- Recalls: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026; MAUDE to Sep 30, 2026

## Decisions per year (last 10)
- 2017: 1
- 2019: 1
- 2023: 1
- 2025: 1

## Most-cited predicates
- K192271: Access PCT, Access PCT Calibrators (2019), cited by 1

Source page: https://510kreport.com/product-code/PTF
Data by year (CSV): https://510kreport.com/product-code/PTF.csv