510(k) Report

FDA applicant

Camp Intl., Inc.

Grand Rapids, MI2 decisions1994–19950 recalls

FDA records 2 decisions for Camp Intl., Inc. (Grand Rapids, MI) from 1994 to 1995: 2 510(k) clearances. Most are in product codes DQX (Wire, Guide, Catheter) and INW (Table, Mechanical). 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 Camp Intl., Inc.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for Camp Intl., Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

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

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Which product codes does it file in?

  • DQXWire, Guide, Catheter1decision
  • INWTable, Mechanical1decision

Who builds on its devices?

Later devices cite its devices 1 time; 0 of those are its own. The firms that cite it most:

Which of its devices are cited most?

Its devices that later submissions most often claim equivalence to.

  • K935998EnterpriseCamp Intl., Inc. · 19951cites it

What has FDA decided for it lately?

  • K935998EnterpriseCamp Intl., Inc. · 1995
  • K940238Tumble Forms Junior TristanderCamp Intl., Inc. · 1994

All 2 as Camp Intl., Inc. →

Other applicant names beginning “Camp”

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

Camp Contact Lenses 1