FDA applicant
Physicians Digital Co.
FDA records 2 decisions for Physicians Digital Co. (Richmond, CA) from 1989 to 1990: 2 510(k) clearances. Most are in product codes IKK (System, Isokinetic Testing And Evaluation) and KQX (Goniometer, Ac-Powered). No recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Physicians Digital Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Physicians Digital Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Physicians Digital Co.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
See the 510(k) ReportOther applicant names beginning “Physicians”
FDA records each applicant name separately; these may or may not be the same firm.