Deepview Digital Video Physiological Portable Imaging System

FDA 510(k) K124049 · Spectralmd, Inc.

Substantially Equivalent

510(k) numberK124049

Submission

Device name
Deepview Digital Video Physiological Portable Imaging System
Applicant
Spectralmd, Inc.
Richardson, TX, US
Received
December 31, 2012
Decision date
April 18, 2013
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
DPT – Probe, Blood-Flow, Extravascular
Device class
Class II (moderate risk)
Regulation
21 CFR 870.2120
Specialty
Cardiovascular

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Questions and answers

When was Deepview Digital Video Physiological Portable Imaging System cleared by the FDA?

Deepview Digital Video Physiological Portable Imaging System (K124049) received a 510(k) decision of Substantially Equivalent on April 18, 2013, 108 days after the submission was received.

What is the product code of K124049?

The FDA product code is DPT – Probe, Blood-Flow, Extravascular, a Class II (moderate risk) device regulated under 21 CFR 870.2120.