Foley & Lardner - FDA 510(k) Cleared Devices

Foley & Lardner, is a top 50 global law firm with a registered facility in Washington, US. The firm provides comprehensive legal services across corporate, intellectual property, and litigation practice areas.

The company received 5 FDA 510(k) clearances from 5 total submissions, with no denied submissions on record. Physical Medicine devices dominated the regulatory portfolio, representing 80% of submissions. Clearances span from 1994 to 1998, with the most recent approval in 1998. The company's Physical Medicine devices included therapeutic and diagnostic equipment. A cardiovascular blood pressure monitoring device was also cleared during this period.

This is a historical regulatory record. No FDA 510(k) clearances have been issued since 1998, indicating the company is no longer active in medical device manufacturing or submission. Explore the complete device names, product codes, and clearance dates in the full database record.