FDA applicant
Cr Tech, Ltd.
FDA records 1 decision for Cr Tech, Ltd. (Baltimore, MD) in 2005: 1 510(k) clearance. All are in product code MQB (Solid State X-Ray Imager (Flat Panel/Digital…). 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 Cr Tech, Ltd.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Cr Tech, Ltd. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Cr Tech, Ltd.’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) Report