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FDA 510(k)

MODEL 520A NOVAMETRIX PULSE OXIMETER

K-Number: K913516 · 1991-11-04

Decision Date1991-11-04
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MODEL 520A NOVAMETRIX PULSE OXIMETER is the device name listed in this FDA 510(k) record. The listed applicant is Novametrix Medical Systems, Inc.. It received FDA 510(k) clearance on 1991-11-04 under 510(k) number K913516. 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 MODEL 520A NOVAMETRIX PULSE OXIMETER?

MODEL 520A NOVAMETRIX PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1991-11-04. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K913516.

When did MODEL 520A NOVAMETRIX PULSE OXIMETER receive FDA 510(k) clearance?

MODEL 520A NOVAMETRIX PULSE OXIMETER received FDA 510(k) clearance on 1991-11-04, under 510(k) number K913516.

Who is the listed applicant for MODEL 520A NOVAMETRIX PULSE OXIMETER?

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

What is the FDA product code for MODEL 520A NOVAMETRIX PULSE OXIMETER?

The FDA product code for MODEL 520A NOVAMETRIX 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 Novametrix Medical Systems, 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 45 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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