FDA applicant
North American Sterilization & Packaging Co.
FDA records 16 decisions for North American Sterilization & Packaging Co. (Sparta, NJ) from 1989 to 1997: 16 510(k) clearances. Most are in product codes LDQ (Unnamed device) and FAS (Electrode, Electrosurgical, Active, Urological). 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 North American Sterilization & Packaging Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for North American Sterilization & Packaging Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like North American Sterilization &…’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