TOWEL CLIPS— 510(k) K890159

Name: FDA 510(k) clearance K890159
Creator: U.S. Food and Drug Administration
Published: 1989-02-03

Substantially Equivalent

Dhason Brothers, Inc.

FDA 510(k) clearance K890159 for TOWEL CLIPS, Substantially Equivalent on 1989-02-03. Applicant: Dhason Brothers, Inc.. Device class: 1.

Clearance details

Applicant: Dhason Brothers, Inc.
Product code: Code GDO
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1989-01-09
Decision date: 1989-02-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hyattsville, MD, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code GDO

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K926199 — UNICLIP SURGICAL CLIP APPLIER1993-04-20
K890941 — MODIFIED SUTURE DISP. ENDOSCOPIC SURGICAL CLIP APP1989-04-07
K890233 — SUTURE CLIP APPLIER/REMOVER1989-01-27
K820837 — DISPOSABLE MULTIPLE LIGATING CLIP1982-05-28
K812291 — ETHICON MULTIPLE LIGATING CLIP APPLIER1981-09-11

More clearances from Dhason Brothers, Inc.

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K890156 — IMPACTOR FOR FEMORAL HEAD1989-02-13
K890157 — FORCEPS1989-02-13
K890158 — RETRACTORS1989-02-13
K890160 — GOUGES FOR FEMORAL HEADS1989-02-13
K890161 — THOMPSON TYPE RASP W/TOMMY BAR1989-02-13

Adverse events under product code GDO

product code GDO

Death: 5
Malfunction: 2,124
Total: 2,129

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.