510(k) Report

FDA applicant

Med-Pro Technologies, Inc.

Appollo Beach, FL1 decision2000–20001 recall

FDA records 1 decision for Med-Pro Technologies, Inc. (Appollo Beach, FL) in 2000: 1 510(k) clearance. All are in product code FMI (Needle, Hypodermic, Single Lumen). 1 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 Med-Pro Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Med-Pro Technologies, Inc. since 2007.

Recalls per year

1in 2016

2016: 1
2007high 1 (2016) · low 0 (2007)2026

Class I Class II/III not classified

FIG. 1 — Med-Pro Technologies, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Which product codes does it file in?

  • FMINeedle, Hypodermic, Single Lumen1decision

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.

  • K000714Vacuflow+Safe Blood Collection Set and Vacuflow+Safe with Holder Blood Collection SetMed-Pro Technologies, Inc. · 20001cites it

What has FDA decided for it lately?

  • K000714Vacuflow+Safe Blood Collection Set and Vacuflow+Safe with Holder Blood Collection SetMed-Pro Technologies, Inc. · 20001 recall

The one decision as Med-Pro Technologies, Inc. →

What has been recalled?

1 recall linked to its devices; the latest:

  • K000714MED 5223 - VacuFlow Safe, Multi-Sample Blood Collection Set With Luer Adapter Tube 12"…Aug 9, 2016Class II