MODIFIED OXYGEN DELIVERY/CO2 SAMPLE NASAL CANNULA
K-Number: K892406 · 1989-07-24
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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