FDA applicant
Medcraft Corp.
FDA records 5 decisions for Medcraft Corp. (Mchenry, IL) from 1976 to 1986: 5 510(k) clearances. Most are in product codes DPS (Electrocardiograph) and DSH (Recorder, Magnetic Tape, Medical). 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 Medcraft Corp.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Medcraft Corp. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Medcraft Corp.’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