device_postmarket_lookup
Retrieve post-clearance intelligence for a medical device by 510(k) number: recalls, MAUDE adverse events, warning letters, 483 matches, and drift signals.
Instructions
Post-clearance intelligence for one AI/ML device by 510(k) number: its product code's recalls, MAUDE adverse-event level and trend, warning-letter and 483 matches for the applicant, plus per-device drift signals (adverse-event inflection, re-clearances of the same device line, software-recall patterns, predicate-cohort recall activity). Descriptive observables with sources — never a safety judgment.
Input Schema
| Name | Required | Description | Default |
|---|---|---|---|
| k_number | Yes | 510(k) or De Novo number, e.g. K252148 or DEN180001 |