Cleared Traditional

PILLING ESOPHAGEAL BOUGIES

K133439 · Teleflexmedical, Inc. · Gastroenterology & Urology
Jun 2014
Decision
216d
Days
Class 2
Risk

About This 510(k) Submission

K133439 is an FDA 510(k) clearance for the PILLING ESOPHAGEAL BOUGIES, a Bougie, Esophageal, And Gastrointestinal, Gastro-urology (Class II — Special Controls, product code FAT), submitted by Teleflexmedical, Inc. (Durham, US). The FDA issued a Cleared decision on June 16, 2014, 216 days after receiving the submission on November 12, 2013. This device falls under the Gastroenterology & Urology review panel. Regulated under 21 CFR 876.5365.

Submission Details

510(k) Number K133439 FDA.gov
FDA Decision Cleared SESE
Date Received November 12, 2013
Decision Date June 16, 2014
Days to Decision 216 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code FAT — Bougie, Esophageal, And Gastrointestinal, Gastro-urology
Device Class Class II — Special Controls
CFR Regulation 21 CFR 876.5365

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