INTESTINAL CLAMP— 510(k) K890372

Name: FDA 510(k) clearance K890372
Creator: U.S. Food and Drug Administration
Published: 1989-02-03

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890372 for INTESTINAL CLAMP, Substantially Equivalent on 1989-02-03. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code HXD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-01-23
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code HXD

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K890368 — KIDNEY CLAMP1989-02-03
K890371 — INTESTINAL CRUSHING CLAMP1989-02-03
K890381 — PARAMETRIUM CLAMP1989-02-03
K874959 — VASCULAR CLAMP1987-12-30
K872386 — C CLAMP1987-07-02

More clearances from Kinetic Medical Products

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K890385 — MIDWIFERY/OBSTETRICAL FORCEPS1989-03-01
K890376 — VAGINAL SPECULUM1989-02-27
K890380 — CERVICAL BIOPSY FORCEPS1989-02-27
K890382 — COMPRESSION FORCEPS1989-02-27
K890387 — MALLEABLE PLACENTA CURETTE1989-02-27

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.