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FDA 510(k)

AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100

K-Number: K052669 · 2005-12-23

Decision Date2005-12-23
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 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 2005-12-23 under 510(k) number K052669. 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 AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100?

AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 is a medical device that received FDA 510(k) clearance on 2005-12-23. The listed applicant is Nonin Medical, Inc.. The 510(k) number is K052669.

When did AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 receive FDA 510(k) clearance?

AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 received FDA 510(k) clearance on 2005-12-23, under 510(k) number K052669.

Who is the listed applicant for AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100?

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 AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100?

The FDA product code for AVANT DIGITAL PULSE OXIMETRY SYSTEM, MODEL 4000, 4100 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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