510(k) Report

FDA applicant

Peritronics Research and Development, Inc.

Arcadia, CA2 decisions1986–19870 recalls

FDA records 2 decisions for Peritronics Research and Development, Inc. (Arcadia, CA) from 1986 to 1987: 2 510(k) clearances. All are in product code HGM (System, Monitoring, Perinatal). 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 Peritronics Research and Development, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Peritronics Research and Development, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Peritronics Research and Development, 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?

  • HGMSystem, Monitoring, Perinatal2decisions

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.

  • K870692Perinatal Computers 2015/2025/2040/2045/2080/2085Peritronics Research and Development, Inc. · 19871cites it

What has FDA decided for it lately?

  • K870692Perinatal Computers 2015/2025/2040/2045/2080/2085Peritronics Research and Development, Inc. · 1987
  • K855044Perinatal Computer Sys Model 100A & 100BPeritronics Research and Development, Inc. · 1986

All 2 as Peritronics Research and Development, Inc. →