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FDA 510(k)

MICROPROCESSOR 7200A VENTILATOR

K-Number: K843424 · 1984-11-01

Decision Date1984-11-01
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MICROPROCESSOR 7200A VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Puritan Bennett Corp.. It received FDA 510(k) clearance on 1984-11-01 under 510(k) number K843424. 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 MICROPROCESSOR 7200A VENTILATOR?

MICROPROCESSOR 7200A VENTILATOR is a medical device that received FDA 510(k) clearance on 1984-11-01. The listed applicant is Puritan Bennett Corp.. The 510(k) number is K843424.

When did MICROPROCESSOR 7200A VENTILATOR receive FDA 510(k) clearance?

MICROPROCESSOR 7200A VENTILATOR received FDA 510(k) clearance on 1984-11-01, under 510(k) number K843424.

Who is the listed applicant for MICROPROCESSOR 7200A VENTILATOR?

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

What is the FDA product code for MICROPROCESSOR 7200A VENTILATOR?

The FDA product code for MICROPROCESSOR 7200A 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 Puritan Bennett 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 110 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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