510(k) Report

FDA applicant

Tower Stopper, Inc.

Hancock, MN1 decision1989–19890 recalls

FDA records 1 decision for Tower Stopper, Inc. (Hancock, MN) in 1989: 1 510(k) clearance. All are in product code BYI (Percussor, Powered-Electric). 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, anesthesiology panel, where it files most

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

FDA decisions per year

No FDA decision for Tower Stopper, Inc. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — Tower Stopper, 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?

  • BYIPercussor, Powered-Electric1decision

What has FDA decided for it lately?

  • K882604Pulmo-PattyTower Stopper, Inc. · 1989

The one decision as Tower Stopper, Inc. →

Other applicant names beginning “Tower”

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

Tower Products, Inc. 3Tower Rubber Industries Sdn. Bhd. 2Tower Laboratories, Ltd. 1Tower Marketing Sdn. Bhd. 1Tower Mfg. Co., Inc. 1