Panoramic Oxygen Mask (POM)

FDA 510(k) K172365 · Pom Medical, LLC

Substantially Equivalent

510(k) numberK172365

Submission

Device name
Panoramic Oxygen Mask (POM)
Applicant
Pom Medical, LLC
Simi Valley, CA, US
Received
August 4, 2017
Decision date
April 19, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1400
Specialty
Anesthesiology

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Questions and answers

When was Panoramic Oxygen Mask (POM) cleared by the FDA?

Panoramic Oxygen Mask (POM) (K172365) received a 510(k) decision of Substantially Equivalent on April 19, 2018, 258 days after the submission was received.

What is the product code of K172365?

The FDA product code is CCK – Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase, a Class II (moderate risk) device regulated under 21 CFR 868.1400.