FDA applicant

Fischer Medical Technologies, Inc.

Denver, CO1 decision2000–20001 recall

FDA records 1 decision for Fischer Medical Technologies, Inc. (Denver, CO) in 2000: 1 510(k) clearance. All are in product code JOQ (Generator, Pulse, Pacemaker, External…). 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, cardiovascular panel, where it files most

How often FDA has decided Fischer Medical Technologies, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Fischer Medical Technologies, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Fischer Medical Technologies, 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 “Fischer”

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

Fischer Imaging Corp. 69 Fischer Industries, Inc. 3 Fischer-Zoth Audiologic Systems, Inc. 2 Fischer Medical 1 Fischer Surgical, Inc. 1

Fischer Medical Technologies, Inc.

Which product codes does it file in?

Who builds on its devices?

Which of its devices are cited most?

What has FDA decided for it lately?

What has been recalled?

Other applicant names beginning “Fischer”