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FDA 510(k)

CONTINUOUS VENTILATOR

K-Number: K840119 · 1984-04-06

Decision Date1984-04-06
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CONTINUOUS VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Bear Medical Systems, Inc.. It received FDA 510(k) clearance on 1984-04-06 under 510(k) number K840119. 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 CONTINUOUS VENTILATOR?

CONTINUOUS VENTILATOR is a medical device that received FDA 510(k) clearance on 1984-04-06. The listed applicant is Bear Medical Systems, Inc.. The 510(k) number is K840119.

When did CONTINUOUS VENTILATOR receive FDA 510(k) clearance?

CONTINUOUS VENTILATOR received FDA 510(k) clearance on 1984-04-06, under 510(k) number K840119.

Who is the listed applicant for CONTINUOUS VENTILATOR?

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

What is the FDA product code for CONTINUOUS VENTILATOR?

The FDA product code for CONTINUOUS 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 Bear Medical Systems, Inc. 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 28 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

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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