FDA applicant

Konigsberg Instruments, Inc.

Walker, MI3 decisions1981–19980 recalls

FDA records 3 decisions for Konigsberg Instruments, Inc. (Walker, MI) from 1981 to 1998: 3 510(k) clearances. Most are in product codes LIT (Catheter, Angioplasty, Peripheral, Transluminal) and FFX (System, Gastrointestinal Motility (Electrical)). 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, gastroenterology and urology panel, where it files most

How often FDA has decided Konigsberg Instruments, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Konigsberg Instruments, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Konigsberg Instruments, Inc.

Which product codes does it file in?

What has FDA decided for it lately?