STRYKER ENDOSCOPY CHOLANGIOGRAM KIT— 510(k) K924212

Name: FDA 510(k) clearance K924212
Creator: U.S. Food and Drug Administration
Published: 1993-07-07

Unknown

Stryker Corp.

FDA 510(k) clearance K924212 for STRYKER ENDOSCOPY CHOLANGIOGRAM KIT, Unknown on 1993-07-07. Applicant: Stryker Corp.. Device class: 1.

Clearance details

Applicant: Stryker Corp.
Product code: Code GBZ
Device class: Class 1
Regulation: 21 CFR 878.4200
Advisory panel: General, Plastic Surgery
Date received: 1992-08-20
Decision date: 1993-07-07
Decision: Unknown
Clearance type: Traditional
Location: San Jose, CA, 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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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.