510(k) Report

FDA applicant

Science Incorporated

Bloomington, MN4 decisions1997–20020 recalls

FDA records 4 decisions for Science Incorporated (Bloomington, MN) from 1997 to 2002: 4 510(k) clearances. Most are in product codes MEB (Pump, Infusion, Elastomeric) and FRN (Pump, Infusion). Its devices cite 4 predicates, 2 of them its own earlier devices. 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 Science Incorporated’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Science Incorporated since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Science Incorporated by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Science”

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