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FDA 510(k)

MODEL AVANT 2120 PULSE OXIMETER AND NIBP

K-Number: K031487 · 2004-03-22

ApplicantNonin Medical, Inc.
Decision Date2004-03-22
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL AVANT 2120 PULSE OXIMETER AND NIBP is the device name listed in this FDA 510(k) record. The listed applicant is Nonin Medical, Inc.. It received FDA 510(k) clearance on 2004-03-22 under 510(k) number K031487. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL AVANT 2120 PULSE OXIMETER AND NIBP?

MODEL AVANT 2120 PULSE OXIMETER AND NIBP is a medical device that received FDA 510(k) clearance on 2004-03-22. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K031487.

When did MODEL AVANT 2120 PULSE OXIMETER AND NIBP receive FDA 510(k) clearance?

MODEL AVANT 2120 PULSE OXIMETER AND NIBP received FDA 510(k) clearance on 2004-03-22, under 510(k) number K031487.

Who is the listed applicant for MODEL AVANT 2120 PULSE OXIMETER AND NIBP?

The FDA 510(k) record lists Nonin Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODEL AVANT 2120 PULSE OXIMETER AND NIBP?

The FDA product code for MODEL AVANT 2120 PULSE OXIMETER AND NIBP is DXN.

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Related Devices (Code: DXN)

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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