510(k) Report

FDA applicant

Vitalab Products Corp.

Mchenry, IL4 decisions1978–19780 recalls

FDA records 4 decisions for Vitalab Products Corp. (Mchenry, IL) in 1978: 4 510(k) clearances. Most are in product codes CAT (Cannula, Nasal, Oxygen) and BYX (Tubing, Pressure And Accessories). 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, anesthesiology panel, where it files most

How often FDA has decided Vitalab Products Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Vitalab Products Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Vitalab Products Corp. 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?

  • CATCannula, Nasal, Oxygen1decision
  • BYXTubing, Pressure And Accessories1decision
  • DPTProbe, Blood-Flow, Extravascular1decision
  • KGBMask, Oxygen, Non-Rebreathing1decision

What has FDA decided for it lately?

  • K781416Tubing, Flexible, Medical GasVitalab Products Corp. · 1978
  • K781415Cannula, Nasal, OxygenVitalab Products Corp. · 1978
  • K781413Mask, PxygenVitalab Products Corp. · 1978
  • K781414Mask, Oxygen, NonbreathingVitalab Products Corp. · 1978

All 4 as Vitalab Products Corp. →