MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA
K-Number: K864903 · 1987-01-30
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Device Summary
Frequently Asked Questions
What is the MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA?
MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA is a medical device that received FDA 510(k) clearance on 1987-01-30. The listed applicant is Salter Labs. The 510(k) number is K864903.
When did MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA receive FDA 510(k) clearance?
MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA received FDA 510(k) clearance on 1987-01-30, under 510(k) number K864903.
Who is the listed applicant for MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. 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 MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. CANNULA?
The FDA product code for MOD. 4006 ADU., OXY. DELIVE.-ORAL CO2 SAM. 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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