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FDA 510(k)

P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER

K-Number: K883038 · 1988-11-16

Decision Date1988-11-16
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

P/N 9320 LOW FLOW AIR/OXYGEN 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 1988-11-16 under 510(k) number K883038. 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 P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER?

P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER is a medical device that received FDA 510(k) clearance on 1988-11-16. The listed applicant is Bird Products Corp.. The 510(k) number is K883038.

When did P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER receive FDA 510(k) clearance?

P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER received FDA 510(k) clearance on 1988-11-16, under 510(k) number K883038.

Who is the listed applicant for P/N 9320 LOW FLOW AIR/OXYGEN 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 P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER?

The FDA product code for P/N 9320 LOW FLOW AIR/OXYGEN MICROBLENDER is BZR.

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: 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.

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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