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)

JOHN BUNN: MEDIX COMPACT TRAVELLER

K-Number: K900854 · 1990-04-23

ApplicantThe John Bunn Co.
Decision Date1990-04-23
Product CodeBTT
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

JOHN BUNN: MEDIX COMPACT TRAVELLER 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 1990-04-23 under 510(k) number K900854. The device is classified under product code BTT. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the JOHN BUNN: MEDIX COMPACT TRAVELLER?

JOHN BUNN: MEDIX COMPACT TRAVELLER is a medical device that received FDA 510(k) clearance on 1990-04-23. The listed applicant is The John Bunn Co.. The 510(k) number is K900854.

When did JOHN BUNN: MEDIX COMPACT TRAVELLER receive FDA 510(k) clearance?

JOHN BUNN: MEDIX COMPACT TRAVELLER received FDA 510(k) clearance on 1990-04-23, under 510(k) number K900854.

Who is the listed applicant for JOHN BUNN: MEDIX COMPACT TRAVELLER?

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 JOHN BUNN: MEDIX COMPACT TRAVELLER?

The FDA product code for JOHN BUNN: MEDIX COMPACT TRAVELLER is BTT.

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.

K883216BUNN MODEL 50 OXYGEN FLOW CONTROLLERK873071BUNN CONCENTRATOR MODEL 2100 SERIESK870094BUNN 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: BTT)

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.

K262268Optiflow Oxygen Kit (AA484J)Fisher and Paykel Healthcare LimitedK254078HVT 2.0Vapotherm, Inc.K251448FL-10000U Respiratory HumidifierFlexicare Medical Limited.K251419Laboratorios Biogalenic Sterile Water for Inhalation, USPLaboratorios Biogalenic S.A. DE C.V.K253479Optiflow Switch+ Filtered Nasal Interface with CO2 Sampling (AA042J)Fisher & Paykel Healthcare, Ltd.K250312Hudson RCI® Comfort Flo Nasal Cannula Premature, Infant; Hudson RCI® Comfort Flo Plus and Soft Plus Cannula Extra SmallMedline Industries, LP

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.

↑