510(k) Report

FDA applicant

Instrument Technology, Inc.

Mountain View, CA2 decisions1985–19860 recalls

FDA records 2 decisions for Instrument Technology, Inc. (Mountain View, CA) from 1985 to 1986: 2 510(k) clearances. All are in product code KNG (Monitor, Ultrasonic, Fetal). 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, obstetrics and gynecology panel, where it files most

How often FDA has decided Instrument Technology, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Instrument Technology, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Instrument Technology, 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?

  • KNGMonitor, Ultrasonic, Fetal1decision

What has FDA decided for it lately?

  • K852655CombiscopeInstrument Technology, Inc. · 1986
  • K850388Iti 200 Electric Motor Drive, Univ.-Wheelchair AccInstrument Technology, Inc. · 1985

All 2 as Instrument Technology, Inc. →

Other applicant names beginning “Instrument”

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

Instrument Makar, Inc. 28Instrument AB Scanditronix 1Instrument Development Corp. 1