Modification to Merits Health Products Oxygen Concentrators

FDA 510(k) K014301 · Merits Health Products Co., Ltd.

Substantially Equivalent

510(k) numberK014301

Submission

Device name
Modification to Merits Health Products Oxygen Concentrators
Applicant
Merits Health Products Co., Ltd.
Fort Myers, FL, US
Received
December 31, 2001
Decision date
February 11, 2002
Decision
Substantially Equivalent (SESE)
Type
Special 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 Modification to Merits Health Products Oxygen Concentrators cleared by the FDA?

Modification to Merits Health Products Oxygen Concentrators (K014301) received a 510(k) decision of Substantially Equivalent on February 11, 2002, 42 days after the submission was received.

What is the product code of K014301?

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