Mark 5 Nuvo Lite Ocsi and STD

FDA 510(k) K082566 · Nidek Medical Products, Inc.

Substantially Equivalent

510(k) numberK082566

Submission

Device name
Mark 5 Nuvo Lite Ocsi and STD
Applicant
Nidek Medical Products, Inc.
Birmingham, AL, US
Received
September 4, 2008
Decision date
December 3, 2008
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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K032509Mark 5 Nuvo (M5C5)CAW · Traditional 03/18/2004SE
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Questions and answers

When was Mark 5 Nuvo Lite Ocsi and STD cleared by the FDA?

Mark 5 Nuvo Lite Ocsi and STD (K082566) received a 510(k) decision of Substantially Equivalent on December 3, 2008, 90 days after the submission was received.

What is the product code of K082566?

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