meddevicedb.com FDA Device Reference

COMINED STANDARD SOLUTION

K130100 Class II Traditional
Decision Date
2013-04-18
Sponsor / Applicant
Mesa Laboratories, Inc.

Technical Specification

510(k) Submission ID K130100
Product Code FKH
Medical Specialty / Panel Gastroenterology, Urology
Regulation Citation 21 CFR 876.5820
Decision Date 2013-04-18
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

COMINED STANDARD SOLUTION received FDA 510(k) clearance under submission number K130100, sponsored by Mesa Laboratories, 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 2013-04-18.

Classification & Regulation

This clearance is catalogued under FDA product code FKH and 21 CFR 876.5820, within the Gastroenterology, Urology review panel as a Class II device.