GIZMO TOWEL CLAMP— 510(k) K791289

Name: FDA 510(k) clearance K791289
Creator: U.S. Food and Drug Administration
Published: 1979-07-24

Substantially Equivalent

Hemoy, Inc.

FDA 510(k) clearance K791289 for GIZMO TOWEL CLAMP, Substantially Equivalent on 1979-07-24. Applicant: Hemoy, Inc.. Device class: 1.

Clearance details

Applicant: Hemoy, Inc.
Product code: Code HXD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1979-07-10
Decision date: 1979-07-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K890371 — INTESTINAL CRUSHING CLAMP1989-02-03
K890372 — INTESTINAL CLAMP1989-02-03
K890381 — PARAMETRIUM CLAMP1989-02-03
K874959 — VASCULAR CLAMP1987-12-30

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K791288 — YELLOW ALERT SYSTEM1979-08-03

Adverse events under product code HXD

product code HXD

Malfunction: 660
Total: 660

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.