ANESTHESIA VENTILATOR CIRCUIT
K-Number: K840850 · 1984-03-19
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Device Summary
Frequently Asked Questions
What is the ANESTHESIA VENTILATOR CIRCUIT?
ANESTHESIA VENTILATOR CIRCUIT is a medical device that received FDA 510(k) clearance on 1984-03-19. The listed applicant is The Kendal Co.. The 510(k) number is K840850.
When did ANESTHESIA VENTILATOR CIRCUIT receive FDA 510(k) clearance?
ANESTHESIA VENTILATOR CIRCUIT received FDA 510(k) clearance on 1984-03-19, under 510(k) number K840850.
Who is the listed applicant for ANESTHESIA VENTILATOR CIRCUIT?
The FDA 510(k) record lists The Kendal Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANESTHESIA VENTILATOR CIRCUIT?
The FDA product code for ANESTHESIA VENTILATOR CIRCUIT is CAI.
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 The Kendal Co. 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: CAI)
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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