510(k) Report

FDA applicant

Perrymeter Systems

Philadelphia, PA1 decision1991–19910 recalls

FDA records 1 decision for Perrymeter Systems (Philadelphia, PA) in 1991: 1 510(k) clearance. All are in product code HIR (Perineometer). 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 Perrymeter Systems’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Perrymeter Systems since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Perrymeter Systems 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?

  • HIRPerineometer1decision

Who builds on its devices?

Later devices cite its devices 2 times; 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.

  • K911190Perrymeter (TM)Perrymeter Systems · 19912cite it

What has FDA decided for it lately?

  • K911190Perrymeter (TM)Perrymeter Systems · 1991

The one decision as Perrymeter Systems →