510(k) Report

FDA applicant

Cavro Scientific Instruments, Inc.

Sunnyvale, CA3 decisions1982–19970 recalls

FDA records 3 decisions for Cavro Scientific Instruments, Inc. (Sunnyvale, CA) from 1982 to 1997: 3 510(k) clearances. All are in product code JQW (Station, Pipetting And Diluting, For Clinical…). 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, clinical chemistry panel, where it files most

How often FDA has decided Cavro Scientific Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Cavro Scientific Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Cavro Scientific 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?

  • JQWStation, Pipetting And Diluting, For Clinical Use3decisions

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.

  • K970616Mini Sampler ProcessorCavro Scientific Instruments, Inc. · 19971cites it

What has FDA decided for it lately?

  • K970616Mini Sampler ProcessorCavro Scientific Instruments, Inc. · 1997
  • K962859Mini Sample ProcessorCavro Scientific Instruments, Inc. · 1996
  • K822208Cavro IQ-190 Sample ProcessorCavro Scientific Instruments, Inc. · 1982

All 3 as Cavro Scientific Instruments, Inc. →