JETPREP FLUSHING DEVICE OL-103037, JETPREP FLUSHING DEVICE OL-133037, JETPREP FLUSHING DEVICE OL-168037, JETPREP FLUSHIN— 510(k) K122740

Name: FDA 510(k) clearance K122740
Creator: U.S. Food and Drug Administration
Published: 2012-12-10

Substantially Equivalent

Jetprep, Ltd.

FDA 510(k) clearance K122740 for JETPREP FLUSHING DEVICE OL-103037, JETPREP FLUSHING DEVICE OL-133037, JETPREP FLUSHING DEVICE OL-168037, JETPREP FLUSHIN, Substantially Equivalent on 2012-12-10. Applicant: Jetprep, Ltd.. Device class: 2.

Clearance details

Applicant: Jetprep, Ltd.
Product code: Code OCX
Device class: Class 2
Regulation: 21 CFR 876.1500
Advisory panel: Gastroenterology, Urology
Date received: 2012-09-06
Decision date: 2012-12-10
Decision: Substantially Equivalent
Clearance type: Special
Location: Washington, DC, US

Download summary PDF View on FDA.gov ↗

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