510(k) Report

FDA applicant

Dermatology Assoc.

Hunt Valley, MD1 decision1995–19950 recalls

FDA records 1 decision for Dermatology Assoc. (Hunt Valley, MD) in 1995: 1 510(k) clearance. All are in product code JOM (Plethysmograph, Photoelectric, Pneumatic Or…). 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 Dermatology Assoc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Dermatology Assoc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Dermatology Assoc. 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?

  • JOMPlethysmograph, Photoelectric, Pneumatic Or Hydraulic1decision

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.

  • K944395Elcat D-PPG, Plethysmograph DeviceDermatology Assoc. · 19951cites it

What has FDA decided for it lately?

  • K944395Elcat D-PPG, Plethysmograph DeviceDermatology Assoc. · 1995

The one decision as Dermatology Assoc. →