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FDA 510(k)

MODIFICATION TO AVANT 9600 PULSE OXIMETER

K-Number: K040589 · 2004-06-03

Decision Date2004-06-03
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO AVANT 9600 PULSE OXIMETER 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 2004-06-03 under 510(k) number K040589. The device is classified under product code DQA. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO AVANT 9600 PULSE OXIMETER?

MODIFICATION TO AVANT 9600 PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 2004-06-03. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K040589.

When did MODIFICATION TO AVANT 9600 PULSE OXIMETER receive FDA 510(k) clearance?

MODIFICATION TO AVANT 9600 PULSE OXIMETER received FDA 510(k) clearance on 2004-06-03, under 510(k) number K040589.

Who is the listed applicant for MODIFICATION TO AVANT 9600 PULSE OXIMETER?

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 MODIFICATION TO AVANT 9600 PULSE OXIMETER?

The FDA product code for MODIFICATION TO AVANT 9600 PULSE OXIMETER is DQA.

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Nonin Medical, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 47 devices →

Related Devices (Code: DQA)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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

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