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FDA 510(k)

NOVAMETRIX MODEL 505 PULSE OXIMETER

K-Number: K873078 · 1987-09-23

Decision Date1987-09-23
Product CodeDQA
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

NOVAMETRIX MODEL 505 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 1987-09-23 under 510(k) number K873078. 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 NOVAMETRIX MODEL 505 PULSE OXIMETER?

NOVAMETRIX MODEL 505 PULSE OXIMETER is a medical device that received FDA 510(k) clearance on 1987-09-23. The listed applicant is Novametrix Medical Systems, Inc.. The 510(k) number is K873078.

When did NOVAMETRIX MODEL 505 PULSE OXIMETER receive FDA 510(k) clearance?

NOVAMETRIX MODEL 505 PULSE OXIMETER received FDA 510(k) clearance on 1987-09-23, under 510(k) number K873078.

Who is the listed applicant for NOVAMETRIX MODEL 505 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 NOVAMETRIX MODEL 505 PULSE OXIMETER?

The FDA product code for NOVAMETRIX MODEL 505 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.

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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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