VENTLAB ANESTHESIA CIRCUIT AC 6000
K-Number: K896897 · 1990-01-26
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Device Summary
Frequently Asked Questions
What is the VENTLAB ANESTHESIA CIRCUIT AC 6000?
VENTLAB ANESTHESIA CIRCUIT AC 6000 is a medical device that received FDA 510(k) clearance on 1990-01-26. The listed applicant is Ventlab Corp.. The 510(k) number is K896897.
When did VENTLAB ANESTHESIA CIRCUIT AC 6000 receive FDA 510(k) clearance?
VENTLAB ANESTHESIA CIRCUIT AC 6000 received FDA 510(k) clearance on 1990-01-26, under 510(k) number K896897.
Who is the listed applicant for VENTLAB ANESTHESIA CIRCUIT AC 6000?
The FDA 510(k) record lists Ventlab Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VENTLAB ANESTHESIA CIRCUIT AC 6000?
The FDA product code for VENTLAB ANESTHESIA CIRCUIT AC 6000 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 Ventlab 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: 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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