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Peralta Stone Removal Catheter

K190492 Class II Traditional
Decision Date
2019-07-18
Sponsor / Applicant
Calcula Technologies, Inc.

Technical Specification

510(k) Submission ID K190492
Product Code FFL
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.4680
Decision Date 2019-07-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Peralta Stone Removal Catheter received FDA 510(k) clearance under submission number K190492, sponsored by Calcula Technologies, 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 2019-07-18.

Classification & Regulation

This clearance is catalogued under FDA product code FFL and 21 CFR 876.4680, within the Gastroenterology, Urology review panel as a Class II device.