meddevicedb.com FDA Device Reference

Bactisure Wound Lavage

K192349 Class II Traditional
Decision Date
2020-01-23
Sponsor / Applicant
Next Science, LLC

Technical Specification

510(k) Submission ID K192349
Product Code FQH
Medical Specialty / Panel General Hospital
Regulation Citation 21 CFR 880.5475
Decision Date 2020-01-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

Bactisure Wound Lavage received FDA 510(k) clearance under submission number K192349, sponsored by Next Science, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the General Hospital review panel. The statutory decision date of record is 2020-01-23.

Classification & Regulation

This clearance is catalogued under FDA product code FQH and 21 CFR 880.5475, within the General Hospital review panel as a Class II device.