ARTERY FORCEPS— 510(k) K890246

Name: FDA 510(k) clearance K890246
Creator: U.S. Food and Drug Administration
Published: 1989-01-27

Substantially Equivalent

Kinetic Medical Products

FDA 510(k) clearance K890246 for ARTERY FORCEPS, Substantially Equivalent on 1989-01-27. Applicant: Kinetic Medical Products. Device class: 1.

Clearance details

Applicant: Kinetic Medical Products
Product code: Code HTD
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-01-18
Decision date: 1989-01-27
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Erie, PA, US

Download summary PDF View on FDA.gov ↗

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K051281 — THE NEEDLE CATCHER2005-09-08
K974593 — SEMKIN INSULATED BIPOLAR FORCEP1998-06-24
K974594 — SEMKIN BIPOLAR FORCEP1998-06-24
K974595 — CUSHING BAYONET, INSULATED BIPOLAR FORCEP1998-06-24
K913964 — MARLOW/REDDICK LAPAROSCOPIC GRASPING FORCEPS1991-10-23

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 HTD

product code HTD

Malfunction: 892
Total: 892

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.