FDA applicant
Hospicare, Inc.
FDA records 1 decision for Hospicare, Inc. (Lake Forest, IL) in 2005: 1 510(k) clearance. All are in product code MRZ (Accessories, Pump, Infusion). Its devices cite 1 predicate, 0 of them its own earlier devices. 1 recall is linked to its devices.
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly
How often FDA has decided Hospicare, Inc.’s devices, and how often a recall has named them.
FDA decisions per year
No FDA decision for Hospicare, Inc. since 2007.
Recalls per year
1in 2012
2007high 1 (2012) · low 0 (2007)2026
Class I Class II/III not classified
Planning a device like Hospicare, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.
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