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FDA 510(k)

VENTLAB ANESTHESIA CIRCUIT AC 6000

K-Number: K896897 · 1990-01-26

ApplicantVentlab Corp.
Decision Date1990-01-26
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLAB ANESTHESIA CIRCUIT AC 6000 is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1990-01-26 under 510(k) number K896897. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 22 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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