FDA applicant

Jomed Catheter, Inc.

Queensbury, NY1 decision2002–20020 recalls

FDA records 1 decision for Jomed Catheter, Inc. (Queensbury, NY) in 2002: 1 510(k) clearance. All are in product code DQY (Catheter, Percutaneous). 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 Jomed Catheter, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Jomed Catheter, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Other applicant names beginning “Jomed”

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

Jomed, Inc. 9 Jomed Imaging, Ltd. 1

Jomed Catheter, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Jomed”