FDA applicant

Paraspinal Diagnostic Corp.

Rockville, MD1 decision1999–19991 recall

FDA records 1 decision for Paraspinal Diagnostic Corp. (Rockville, MD) in 1999: 1 510(k) clearance. All are in product code IKN (Electromyograph, Diagnostic). 1 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, physical medicine panel, where it files most

How often FDA has decided Paraspinal Diagnostic Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Paraspinal Diagnostic Corp. since 2007.

Recalls per year

1in 2010

2007high 1 (2010) · low 0 (2007)2026

Class I Class II/III not classified

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

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Paraspinal Diagnostic Corp.

Which product codes does it file in?

What has FDA decided for it lately?

What has been recalled?