510(k) Report

FDA applicant

Tico Medical Instruments, Inc.

Cocoa, FL4 decisions1984–19910 recalls

FDA records 4 decisions for Tico Medical Instruments, Inc. (Cocoa, FL) from 1984 to 1991: 4 510(k) clearances. Most are in product codes FPA (Set, Administration, Intravascular) and FIB (Protector, Transducer, Dialysis). 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 Tico Medical Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Tico Medical Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tico Medical Instruments, 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?

  • FPASet, Administration, Intravascular2decisions
  • FIBProtector, Transducer, Dialysis1decision
  • DSKComputer, Blood-Pressure1decision

What has FDA decided for it lately?

  • K911658Dialysis Trandsducer ProtectorTico Medical Instruments, Inc. · 1991
  • K884938Vital Signs MonitorTico Medical Instruments, Inc. · 1989
  • K842985T- Extension Set T-04-CTico Medical Instruments, Inc. · 1984
  • K840443Retrograde Infusion Set 3ML & 6ML-Tico Medical Instruments, Inc. · 1984

All 4 as Tico Medical Instruments, Inc. →