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AMT Low-Profile Suprapubic Catheter & Drainage Set

K240514 Class II Traditional
Decision Date
2024-11-01
Sponsor / Applicant
Applied Medical Technology, Inc.

Technical Specification

510(k) Submission ID K240514
Product Code KOB
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5090
Decision Date 2024-11-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

AMT Low-Profile Suprapubic Catheter & Drainage Set received FDA 510(k) clearance under submission number K240514, sponsored by Applied Medical Technology, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Gastroenterology, Urology review panel. The statutory decision date of record is 2024-11-01.

Classification & Regulation

This clearance is catalogued under FDA product code KOB and 21 CFR 876.5090, within the Gastroenterology, Urology review panel as a Class II device.