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FDA 510(k)

BUNN MODEL 22 OXYGEN FLOW CONTROLLER

K-Number: K861199 · 1986-08-26

ApplicantThe John Bunn Co.
Decision Date1986-08-26
Product CodeNFB
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BUNN MODEL 22 OXYGEN FLOW CONTROLLER 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 1986-08-26 under 510(k) number K861199. The device is classified under product code NFB. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BUNN MODEL 22 OXYGEN FLOW CONTROLLER?

BUNN MODEL 22 OXYGEN FLOW CONTROLLER is a medical device that received FDA 510(k) clearance on 1986-08-26. The listed applicant is The John Bunn Co.. The 510(k) number is K861199.

When did BUNN MODEL 22 OXYGEN FLOW CONTROLLER receive FDA 510(k) clearance?

BUNN MODEL 22 OXYGEN FLOW CONTROLLER received FDA 510(k) clearance on 1986-08-26, under 510(k) number K861199.

Who is the listed applicant for BUNN MODEL 22 OXYGEN FLOW CONTROLLER?

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 MODEL 22 OXYGEN FLOW CONTROLLER?

The FDA product code for BUNN MODEL 22 OXYGEN FLOW CONTROLLER is NFB.

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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.

K900854JOHN BUNN: MEDIX COMPACT TRAVELLERK883216BUNN MODEL 50 OXYGEN FLOW CONTROLLERK873071BUNN CONCENTRATOR MODEL 2100 SERIESK870094BUNN MODEL 530 ASPIRATORK861435BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVEK862628BUNN MODEL 510 MEDICATION COMPRESSOR

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Related Devices (Code: NFB)

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.

K250322Respond OC Conserving Regulator (130-0800)Responsive RespiratoryK220591ProximaDynasthetics, LLCK221014Effortless Oxygen Conserver System Models Effortless Pro and Effortless MobileEffortless Oxygen, LLCK200401ApogeeIncoba Ltd D/B/A DynarisK151506Demand Nasal Oxygen Cannula, Modified Demand Nasal Oxygen CannulaSalter LabsK131023THERAFLOW SINGLE LUMEN AND THERAFLOW DUAL LUMENMedical Products, LLC

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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