FDA applicant

Comet Ltd. C/O Radiology Resources, Inc.

Switzerland, CH5 decisions1987–19910 recalls

FDA records 5 decisions for Comet Ltd. C/O Radiology Resources, Inc. (Switzerland, CH) from 1987 to 1991: 5 510(k) clearances. Most are in product codes ITY (Assembly, Tube Housing, X-Ray, Diagnostic) and JAA (System, X-Ray, Fluoroscopic, Image-Intensified). 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, radiology panel, where it files most

How often FDA has decided Comet Ltd. C/O Radiology Resources, Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Comet Ltd. C/O Radiology Resources, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Comet Ltd. C/O Radiology Resources, Inc. by year, 2007–2026Sources: FDA decision databases, recall and enforcement reports · Data through Oct 25, 2026

Planning a device like Comet Ltd. C/O Radiology Resources, Inc.’s? A 510(k) Report ranks candidate predicates for your device by lineage, citations and recall history, with the review-time outlook.

See the 510(k) Report

Other applicant names beginning “Comet”

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

Comet North America, Inc. 1

Comet Ltd. C/O Radiology Resources, Inc.

Which product codes does it file in?

What has FDA decided for it lately?

Other applicant names beginning “Comet”