Hill-Rom Primaview Monitor System

FDA 510(k) K013709 · Hill-Rom, Inc.

Substantially Equivalent

510(k) numberK013709

Submission

Device name
Hill-Rom Primaview Monitor System
Applicant
Hill-Rom, Inc.
Batesville, IN, US
Received
November 8, 2001
Decision date
November 16, 2001
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA
Third-party review
Yes

Official FDA 510(k) record

Device classification

Product code
FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology
Device class
Class II (moderate risk)
Regulation
21 CFR 876.1500
Specialty
Gastroenterology, Urology

To allow for visualization of body cavities through an endoscope by projecting images to a monitor.

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Questions and answers

When was Hill-Rom Primaview Monitor System cleared by the FDA?

Hill-Rom Primaview Monitor System (K013709) received a 510(k) decision of Substantially Equivalent on November 16, 2001, 8 days after the submission was received.

What is the product code of K013709?

The FDA product code is FET – Endoscopic Video Imaging System/Component, Gastroenterology-Urology, a Class II (moderate risk) device regulated under 21 CFR 876.1500.