Is it possible to identify all 510k records of medical devices were a `FDA review` or `clinical trials` is available (e.g. https://www.accessdata.fda.gov/scripts/cdrh/cfdocs/cfpmn/pmn.cfm?ID=K151502) using either the API, the dataset (https://open.fda.gov/apis/device/510k/download/) or any other database?

Records with a summary/statement can easily be identified by `statement_or_summary` in the provided dataset.