NCT03437811View on ClinicalTrials.gov

Airway Clearance System (K031876) Phase IV Device Efficacy

CompletedOBSERVATIONAL
Enrollment

16

Participants

Timeline

Start Date

February 28, 2018

Primary Completion Date

November 1, 2019

Study Completion Date

November 1, 2019

Conditions
Cystic Fibrosis, Pulmonary
Interventions
DEVICE

Electro Flo Percussor, Model 5000

FDA 510K K031876 Regulation Number: 21 CFR 868.5665 Regulation Name: Percussor, Powered-Electric Regulation Class: II Product Code: BY1

Trial Locations (1)

92117

MED Systems, Inc., San Diego

Sponsors
All Listed Sponsors
lead

Mack Biotech, Corp.

INDUSTRY