END TIDAL CO2 TUBE
K-Number: K861454 · 1986-05-06
Advertisement
Device Summary
Frequently Asked Questions
What is the END TIDAL CO2 TUBE?
END TIDAL CO2 TUBE is a medical device that received FDA 510(k) clearance on 1986-05-06. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K861454.
When did END TIDAL CO2 TUBE receive FDA 510(k) clearance?
END TIDAL CO2 TUBE received FDA 510(k) clearance on 1986-05-06, under 510(k) number K861454.
Who is the listed applicant for END TIDAL CO2 TUBE?
The FDA 510(k) record lists Sheridan Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for END TIDAL CO2 TUBE?
The FDA product code for END TIDAL CO2 TUBE is BTR.
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 Sheridan Catheter Corp. 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: BTR)
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.
Advertisement