# Clearflow, Inc.

- Location (FDA's records): Anaheim, CA
- FDA decisions: 6 (2015–2021): 6 510(k) clearances
- Product codes: OTK (6)
- Predicates its devices cite: 5 (4 its own); citations of its devices by later devices: 4 (4 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- Clear Catheter Systems: 1 (https://510kreport.com/company/clear-catheter-systems)

## Its most-cited devices
- K163139: PleuraFlow System with FlowGlide (2016), cited by 2
- K150042: PleuraFlow System (2015), cited by 2

## Recent decisions
- K203394: PleuraFlow System with FlowGlide (Mar 2, 2021)
- K191733: The ZIP Accessory Shuttle for PleuraFlow System (Jul 26, 2019)
- K182067: PleuraFlow System with FlowGlide Extra Drainage Length (Aug 14, 2018)
- K163139: PleuraFlow System with FlowGlide (Nov 30, 2016)
- K153681: PleuraFlow System (Jan 20, 2016)
- K150042: PleuraFlow System (Jun 2, 2015)

Source page: https://510kreport.com/company/clearflow