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FDA 510(k)

BIRD 8400TI ADULT VOLUME VENTILATOR

K-Number: K930747 · 1994-02-15

Decision Date1994-02-15
Product CodeCBK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BIRD 8400TI ADULT VOLUME VENTILATOR is the device name listed in this FDA 510(k) record. The listed applicant is Bird Products Corp.. It received FDA 510(k) clearance on 1994-02-15 under 510(k) number K930747. 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 BIRD 8400TI ADULT VOLUME VENTILATOR?

BIRD 8400TI ADULT VOLUME VENTILATOR is a medical device that received FDA 510(k) clearance on 1994-02-15. The listed applicant is Bird Products Corp.. The 510(k) number is K930747.

When did BIRD 8400TI ADULT VOLUME VENTILATOR receive FDA 510(k) clearance?

BIRD 8400TI ADULT VOLUME VENTILATOR received FDA 510(k) clearance on 1994-02-15, under 510(k) number K930747.

Who is the listed applicant for BIRD 8400TI ADULT VOLUME VENTILATOR?

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

What is the FDA product code for BIRD 8400TI ADULT VOLUME VENTILATOR?

The FDA product code for BIRD 8400TI ADULT VOLUME 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 Bird Products 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 35 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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