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FDA 510(k)

VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B

K-Number: K900115 · 1990-02-22

ApplicantVentlab Corp.
Decision Date1990-02-22
Product CodeCAN
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B is the device name listed in this FDA 510(k) record. The listed applicant is Ventlab Corp.. It received FDA 510(k) clearance on 1990-02-22 under 510(k) number K900115. The device is classified under product code CAN. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B?

VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B is a medical device that received FDA 510(k) clearance on 1990-02-22. The listed applicant is Ventlab Corp.. The 510(k) number is K900115.

When did VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B receive FDA 510(k) clearance?

VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B received FDA 510(k) clearance on 1990-02-22, under 510(k) number K900115.

Who is the listed applicant for VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B?

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 EXHALATION MANIFOLD VX-2000 A & VX-2000 B?

The FDA product code for VENTLAB EXHALATION MANIFOLD VX-2000 A & VX-2000 B is CAN.

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Other records listing Ventlab Corp. as applicant

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Related Devices (Code: CAN)

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.

K162811MR Conditional CGA 870Essex Industries, Inc.K080243PORTABLE OXYGEN UNIT SCA900San Cheong Co. , Ltd.K060265REMCORE REMOTE CONTROLLED OXYGEN REGULATORRemcore, Inc.K061785CYL-FIL OXYGEN SYSTEMResponsive Respiratory, Inc.K950777OXYGEN REGULATORMada Medical Products, Inc.K942751VANGUARD SERIES GAS REGULATORSBuckman Co., Inc.

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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