EPM-3300 Video Processor

FDA 510(k) K934918 · Pentax Precision Instrument Corp.

Substantially Equivalent

510(k) numberK934918

Submission

Device name
EPM-3300 Video Processor
Applicant
Pentax Precision Instrument Corp.
Orangeburg, NY, US
Received
October 15, 1993
Decision date
February 7, 1994
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

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 EPM-3300 Video Processor cleared by the FDA?

EPM-3300 Video Processor (K934918) received a 510(k) decision of Substantially Equivalent on February 7, 1994, 115 days after the submission was received.

What is the product code of K934918?

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.