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FDA 510(k)

BUNN LITE OXYGEN CONCENTRATOR

K-Number: K855208 · 1986-02-21

Decision Date1986-02-21
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BUNN LITE OXYGEN CONCENTRATOR 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 1986-02-21 under 510(k) number K855208. The device is classified under product code CAW. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUNN LITE OXYGEN CONCENTRATOR?

BUNN LITE OXYGEN CONCENTRATOR is a medical device that received FDA 510(k) clearance on 1986-02-21. The listed applicant is The John Bunn Co.. The 510(k) number is K855208.

When did BUNN LITE OXYGEN CONCENTRATOR receive FDA 510(k) clearance?

BUNN LITE OXYGEN CONCENTRATOR received FDA 510(k) clearance on 1986-02-21, under 510(k) number K855208.

Who is the listed applicant for BUNN LITE OXYGEN CONCENTRATOR?

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 BUNN LITE OXYGEN CONCENTRATOR?

The FDA product code for BUNN LITE OXYGEN CONCENTRATOR is CAW.

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: CAW)

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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