FDA applicant
Parke-Davis Co.
FDA records 47 decisions for Parke-Davis Co. (Mchenry, IL) from 1976 to 1986: 47 510(k) clearances. Most are in product codes FOZ (Catheter, Intravascular, Therapeutic…) and DYG (Catheter, Flow Directed). 2 recalls are linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Parke-Davis Co.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Parke-Davis Co. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Parke-Davis 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) Report