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FDA 510(k)

LOW FLOW N2O/02O MICROBLENDER

K-Number: K900722 · 1990-07-18

ApplicantBird Products Corp.
Decision Date1990-07-18
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

LOW FLOW N2O/02O MICROBLENDER 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 1990-07-18 under 510(k) number K900722. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LOW FLOW N2O/02O MICROBLENDER?

LOW FLOW N2O/02O MICROBLENDER is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Bird Products Corp.. The 510(k) number is K900722.

When did LOW FLOW N2O/02O MICROBLENDER receive FDA 510(k) clearance?

LOW FLOW N2O/02O MICROBLENDER received FDA 510(k) clearance on 1990-07-18, under 510(k) number K900722.

Who is the listed applicant for LOW FLOW N2O/02O MICROBLENDER?

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 LOW FLOW N2O/02O MICROBLENDER?

The FDA product code for LOW FLOW N2O/02O MICROBLENDER is BZR.

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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.

K032451BIRD TBIRD VELA VENTILATORK022674BIRD AVEA VENTILATORK020730ORION NASAL CPAP SYSTEMK013642AVEAK020746BIRD TBIRD VELA VENTILATORK003770BIRD TBIRD LEGACY VENTILATOR

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Related Devices (Code: BZR)

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.

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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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