Cleared Traditional

K170672 - Tamper Evident Cap For use with ENFit Syringes (FDA 510(k) Clearance)

Oct 2017
Decision
214d
Days
Class 2
Risk

K170672 is an FDA 510(k) clearance for the Tamper Evident Cap For use with ENFit Syringes. This device is classified as a Enteral Syringes With Enteral Specific Connectors (Class II - Special Controls, product code PNR).

Submitted by International Medical Industries, Inc. (Pompano Beach, US). The FDA issued a Cleared decision on October 6, 2017, 214 days after receiving the submission on March 6, 2017.

This device falls under the Gastroenterology & Urology FDA review panel. Regulated under 21 CFR 876.5980. Delivers Nutrition, Medication, Or Hydration Orally Or To A Gastrointestinal Tube Or Extension Set Using Aami/cn3(ps):2014 Compliant Connectors..

Submission Details

510(k) Number K170672 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received March 06, 2017
Decision Date October 06, 2017
Days to Decision 214 days
Submission Type Traditional
Review Panel Gastroenterology & Urology (GU)
Summary Summary PDF

Device Classification

Product Code PNR - Enteral Syringes With Enteral Specific Connectors
Device Class Class II - Special Controls
CFR Regulation 21 CFR 876.5980
Definition Delivers Nutrition, Medication, Or Hydration Orally Or To A Gastrointestinal Tube Or Extension Set Using Aami/cn3(ps):2014 Compliant Connectors.