510(k) Report

FDA applicant

Medication Delivery Devices, Inc.

San Diego, CA1 decision1994–19940 recalls

FDA records 1 decision for Medication Delivery Devices, Inc. (San Diego, CA) in 1994: 1 510(k) clearance. All are in product code FRN (Pump, Infusion). 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 Medication Delivery Devices, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Medication Delivery Devices, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

Planning a device like Medication Delivery Devices, 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

Which product codes does it file in?

  • FRNPump, Infusion1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K931458Medipak Ambulatory Infusion PumpMedication Delivery Devices, Inc. · 19941cites it

What has FDA decided for it lately?

  • K931458Medipak Ambulatory Infusion PumpMedication Delivery Devices, Inc. · 1994

The one decision as Medication Delivery Devices, Inc. →