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FDA 510(k)

MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA

K-Number: K892406 · 1989-07-24

ApplicantSalter Labs
Decision Date1989-07-24
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Salter Labs. It received FDA 510(k) clearance on 1989-07-24 under 510(k) number K892406. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA?

MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA is a medical device that received FDA 510(k) clearance on 1989-07-24. The listed applicant is Salter Labs. The 510(k) number is K892406.

When did MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA receive FDA 510(k) clearance?

MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA received FDA 510(k) clearance on 1989-07-24, under 510(k) number K892406.

Who is the listed applicant for MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA?

The FDA 510(k) record lists Salter Labs as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA?

The FDA product code for MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA is CCK.

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 Salter Labs 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: CCK)

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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