510(k) Report

FDA applicant

Mission Medicl Devices

San Diego, CA1 decision2001–20010 recalls

FDA records 1 decision for Mission Medicl Devices (San Diego, CA) in 2001: 1 510(k) clearance. All are in product code FPA (Set, Administration, Intravascular). 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 Mission Medicl Devices’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Mission Medicl Devices since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Mission”

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