FDA applicant
Perkins Mfg. Co.
FDA records 14 decisions for Perkins Mfg. Co. (Dallas, TX) from 1977 to 1997: 14 510(k) clearances. Most are in product codes JAA (System, X-Ray, Fluoroscopic, Image-Intensified) and IZI (System, X-Ray, Angiographic). 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 Perkins Mfg. Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Perkins Mfg. Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Perkins Mfg. 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 “Perkins”
FDA records each applicant name separately; these may or may not be the same firm.