510(k) Report

FDA applicant

Access / God Loves You

Castle Rock, CO4 decisions1992–19930 recalls

FDA records 4 decisions for Access / God Loves You (Castle Rock, CO) from 1992 to 1993: 4 510(k) clearances. Most are in product codes FRN (Pump, Infusion) and HLJ (Ophthalmoscope, Battery-Powered). No recall is linked to its devices.

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) refreshed weekly, last Nov 3, 2026

FIG. A — Illustration, general hospital panel, where it files most

How often FDA has decided Access / God Loves You’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Access / God Loves You since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Access / God Loves You by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Access / God Loves You’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

Other applicant names beginning “Access”

FDA records each applicant name separately; these may or may not be the same firm.