FDA applicant
Therapac, Inc.
FDA records 1 decision for Therapac, Inc. (Mchenry, IL) in 1980: 1 510(k) clearance. All are in product code JRR (Regulator, Temperature). 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 Therapac, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Therapac, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Therapac, Inc.’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