FDA applicant

Physio-Dyne Industrument Corp.

Massapequa, NY1 decision1986–19860 recalls

FDA records 1 decision for Physio-Dyne Industrument Corp. (Massapequa, NY) in 1986: 1 510(k) clearance. All are in product code DRT (Monitor, Cardiac (Incl. Cardiotachometer &…). 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, cardiovascular panel, where it files most

How often FDA has decided Physio-Dyne Industrument Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Physio-Dyne Industrument Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Physio-Dyne Industrument Corp. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

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Other applicant names beginning “Physio-Dyne”

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

Physio-Control Corp. 97 Physio Technology, Inc. 10 Physio Systems, Inc. 3 Physio Tronics Corp. 1 Physio Designs, Inc. 1 Physio-Dyne 1 Physio-Dyne Instrument Corp. 1 Physio, Inc. 1 Physio Ventures, Inc. 1

Physio-Dyne Industrument Corp.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Physio-Dyne”