Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

ARIZONA OXYGEN TIMER DEVICE

K-Number: K761260 · 1976-12-16

Decision Date1976-12-16
Product CodeBXP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

ARIZONA OXYGEN TIMER DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is The John Bunn Co.. It received FDA 510(k) clearance on 1976-12-16 under 510(k) number K761260. The device is classified under product code BXP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARIZONA OXYGEN TIMER DEVICE?

ARIZONA OXYGEN TIMER DEVICE is a medical device that received FDA 510(k) clearance on 1976-12-16. The listed applicant is The John Bunn Co.. The 510(k) number is K761260.

When did ARIZONA OXYGEN TIMER DEVICE receive FDA 510(k) clearance?

ARIZONA OXYGEN TIMER DEVICE received FDA 510(k) clearance on 1976-12-16, under 510(k) number K761260.

Who is the listed applicant for ARIZONA OXYGEN TIMER DEVICE?

The FDA 510(k) record lists The John Bunn Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ARIZONA OXYGEN TIMER DEVICE?

The FDA product code for ARIZONA OXYGEN TIMER DEVICE is BXP.

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 The John Bunn Co. 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 20 devices →

Related Devices (Code: BXP)

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.

↑