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)

BUNN CONCENTRATOR MODEL 2100 SERIES

K-Number: K873071 · 1987-09-15

ApplicantThe John Bunn Co.
Decision Date1987-09-15
Product CodeCAW
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

BUNN CONCENTRATOR MODEL 2100 SERIES 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 1987-09-15 under 510(k) number K873071. 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 CONCENTRATOR MODEL 2100 SERIES?

BUNN CONCENTRATOR MODEL 2100 SERIES is a medical device that received FDA 510(k) clearance on 1987-09-15. The listed applicant is The John Bunn Co.. The 510(k) number is K873071.

When did BUNN CONCENTRATOR MODEL 2100 SERIES receive FDA 510(k) clearance?

BUNN CONCENTRATOR MODEL 2100 SERIES received FDA 510(k) clearance on 1987-09-15, under 510(k) number K873071.

Who is the listed applicant for BUNN CONCENTRATOR MODEL 2100 SERIES?

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 CONCENTRATOR MODEL 2100 SERIES?

The FDA product code for BUNN CONCENTRATOR MODEL 2100 SERIES 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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

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 CONTROLLERK870094BUNN MODEL 530 ASPIRATORK861435BUNN CONCENTRATOR MODEL 2011 WITH DEMAND VALVEK861199BUNN MODEL 22 OXYGEN FLOW CONTROLLERK862628BUNN MODEL 510 MEDICATION COMPRESSOR

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.

K254289Portable Oxygen Concentrator (OX-1A-E, OX-1B)Oxytek Medical Technology Co., Ltd.K260171Portable Oxygen Concentrator (PO1 5B, PO1 6B)BMC Medical Co., Ltd.K252399Portable Oxygen ConcentratorHonsun (Nantong) Co., Ltd.K252965Oxygen Concentrator (OX-5A, OX-5C)Oxytek Medical Technology Co., Ltd.K252407OxyGo Portable Oxygen Concentrator (1400-7000)Mv Life, LLCK253549DeVilbiss 5 Liter Oxygen Concentrator (555)Devilbiss Healthcare, 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.

↑