P.R.G. GUIDEWIRE PLACEMENT SYSTEM— 510(k) K903036

Unknown

Applied Medical Technologies

FDA 510(k) clearance K903036 for P.R.G. GUIDEWIRE PLACEMENT SYSTEM, Unknown on 1990-11-19. Applicant: Applied Medical Technologies.

Clearance details

Applicant: Applied Medical Technologies
Product code: Code KGC
Advisory panel: Gastroenterology, Urology
Date received: 1990-07-11
Decision date: 1990-11-19
Decision: Unknown
Clearance type: Traditional
Location: Independence, OH, US

Download summary PDF View on FDA.gov ↗

Adverse events under product code KGC

product code KGC

Death: 7
Total: 7

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.