Mesa II Oxygen Concentrator Model: T2000 Series

FDA 510(k) K100920 · Sequal Technologies Co., Ltd.

Substantially Equivalent

510(k) numberK100920

Submission

Device name
Mesa II Oxygen Concentrator Model: T2000 Series
Applicant
Sequal Technologies Co., Ltd.
Taipei, TW
Received
April 2, 2010
Decision date
November 29, 2010
Decision
Substantially Equivalent (SESE)
Type
Abbreviated 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
CAW – Generator, Oxygen, Portable
Device class
Class II (moderate risk)
Regulation
21 CFR 868.5440
Specialty
Anesthesiology

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Questions and answers

When was Mesa II Oxygen Concentrator Model: T2000 Series cleared by the FDA?

Mesa II Oxygen Concentrator Model: T2000 Series (K100920) received a 510(k) decision of Substantially Equivalent on November 29, 2010, 241 days after the submission was received.

What is the product code of K100920?

The FDA product code is CAW – Generator, Oxygen, Portable, a Class II (moderate risk) device regulated under 21 CFR 868.5440.