510(k) Report

FDA applicant

Automata Medical Instrumentation, Inc.

Scottsdale, AZ2 decisions1993–19960 recalls

FDA records 2 decisions for Automata Medical Instrumentation, Inc. (Scottsdale, AZ) from 1993 to 1996: 2 510(k) clearances. All are in product code FIZ (Meter, Conductivity, Non-Remote). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Automata Medical Instrumentation, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Automata Medical Instrumentation, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Automata Medical Instrumentation, 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?

  • FIZMeter, Conductivity, Non-Remote2decisions

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.

  • K955298Phoenix Dialysate MeterAutomata Medical Instrumentation, Inc. · 19961cites it

What has FDA decided for it lately?

  • K955298Phoenix Dialysate MeterAutomata Medical Instrumentation, Inc. · 1996
  • K920810Neo-Stat Dialysate MeterAutomata Medical Instrumentation, Inc. · 1993

All 2 as Automata Medical Instrumentation, Inc. →

Other applicant names beginning “Automata”

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

Automata Instrumentation, Inc. 3Automata, Inc. 2