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FDA 510(k)

MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR

K-Number: K902405 · 1991-03-04

Decision Date1991-03-04
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Mallinckrodt Medical. It received FDA 510(k) clearance on 1991-03-04 under 510(k) number K902405. The device is classified under product code CBK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR?

MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR is a medical device that received FDA 510(k) clearance on 1991-03-04. The listed applicant is Mallinckrodt Medical. The 510(k) number is K902405.

When did MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR receive FDA 510(k) clearance?

MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR received FDA 510(k) clearance on 1991-03-04, under 510(k) number K902405.

Who is the listed applicant for MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR?

The FDA 510(k) record lists Mallinckrodt Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR?

The FDA product code for MALLARD MEDICAL MODEL 2400 ANESTHESIA VENTILATOR is CBK.

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 Mallinckrodt Medical 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 43 devices →

Related Devices (Code: CBK)

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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