510(k) Report

FDA applicant

American Surgical Technologies Corp.

Haverhiill, MA1 decision1992–19920 recalls

FDA records 1 decision for American Surgical Technologies Corp. (Haverhiill, MA) in 1992: 1 510(k) clearance. All are in product code FWF (Camera, Television, Endoscopic, Without Audio). 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, general and plastic surgery panel, where it files most

How often FDA has decided American Surgical Technologies Corp.’s devices, and how often a recall has named them.

FDA decisions per year

No FDA decision for American Surgical Technologies Corp. since 2007.

Recalls per year

No recall linked to its devices since 2007.

FIG. 1 — American Surgical Technologies Corp. 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?

  • FWFCamera, Television, Endoscopic, Without Audio1decision

Who builds on its devices?

Later devices cite its devices 4 times; 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.

  • K9231603DSCOPEAmerican Surgical Technologies Corp. · 19924cite it

What has FDA decided for it lately?

  • K9231603DSCOPEAmerican Surgical Technologies Corp. · 1992

The one decision as American Surgical Technologies Corp. →