ESOPHAGEAL OBTURATOR/TRACHEAL TUBE
K-Number: K875226 · 1988-01-19
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Device Summary
Frequently Asked Questions
What is the ESOPHAGEAL OBTURATOR/TRACHEAL TUBE?
ESOPHAGEAL OBTURATOR/TRACHEAL TUBE is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Sheridan Catheter Corp.. The 510(k) number is K875226.
When did ESOPHAGEAL OBTURATOR/TRACHEAL TUBE receive FDA 510(k) clearance?
ESOPHAGEAL OBTURATOR/TRACHEAL TUBE received FDA 510(k) clearance on 1988-01-19, under 510(k) number K875226.
Who is the listed applicant for ESOPHAGEAL OBTURATOR/TRACHEAL 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 ESOPHAGEAL OBTURATOR/TRACHEAL TUBE?
The FDA product code for ESOPHAGEAL OBTURATOR/TRACHEAL TUBE is CAO.
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: CAO)
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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