CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP— 510(k) K914015

Name: FDA 510(k) clearance K914015
Creator: U.S. Food and Drug Administration
Published: 1991-11-21

Substantially Equivalent

Pilling Co.

FDA 510(k) clearance K914015 for CLEMENT-PILLING CHOLANGIOGRAPHY CATH GUIDE/CLAMP, Substantially Equivalent on 1991-11-21. Applicant: Pilling Co.. Device class: 1.

Clearance details

Applicant: Pilling Co.
Product code: Code GBZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1991-09-09
Decision date: 1991-11-21
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Fort Washington, PA, US

Download summary PDF View on FDA.gov ↗

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K932228 — MICROVASIVE INSURG CHLOANGIOGRAPHIC CATHETER1993-08-10
K926217 — TERUMO ANGIOGRAPHIC CATHETER FOR LAPOROSCOPIC USE1993-07-13

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K925198 — KAISER NO CANNULA THORACOSCOPY/LAPAROSCOPY INSTR1993-02-12
K922971 — NO-SCALPEL VASCETOMY INSTRUMENTS1992-09-23
K911099 — MEHIGAN-PILLING ANGIOSCOPIC VASCULAR INSTRUM. LINE1991-06-25

Adverse events under product code GBZ

product code GBZ

Death: 2
Total: 2

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.