AMT Enteral Transition Adapters

FDA 510(k) K150034 · Applied Medical Technology, Inc.

Substantially Equivalent

510(k) numberK150034

Submission

Device name
AMT Enteral Transition Adapters
Applicant
Applied Medical Technology, Inc.
Brecksville, OH, US
Received
January 9, 2015
Decision date
June 9, 2015
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
PIO – Enteral Specific Transition Connectors
Device class
Class II (moderate risk)
Regulation
21 CFR 876.5980
Specialty
Gastroenterology, Urology

Facilitates enteral specific connections between AAMI/CN3(PS):2014 compliant connectors and non ISO 80369-1 compliant legacy enteral connectors.

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Questions and answers

When was AMT Enteral Transition Adapters cleared by the FDA?

AMT Enteral Transition Adapters (K150034) received a 510(k) decision of Substantially Equivalent on June 9, 2015, 151 days after the submission was received.

What is the product code of K150034?

The FDA product code is PIO – Enteral Specific Transition Connectors, a Class II (moderate risk) device regulated under 21 CFR 876.5980.