FDA applicant
Puritas Health Care, Inc.
FDA records 24 decisions for Puritas Health Care, Inc. (New Milford, CT) from 1991 to 1994: 24 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and BSY (Catheters, Suction, Tracheobronchial). 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 Puritas Health Care, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Puritas Health Care, Inc. since 2007.
Recalls per year
No recall linked to its devices since 2007.
Planning a device like Puritas Health Care, 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