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)

PEAK EXPIRATORY FLOW METER, KN-9710

K-Number: K092335 · 2010-04-09

ApplicantK-Jump Health Co., Ltd.
Decision Date2010-04-09
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

PEAK EXPIRATORY FLOW METER, KN-9710 is the device name listed in this FDA 510(k) record. The listed applicant is K-Jump Health Co., Ltd.. It received FDA 510(k) clearance on 2010-04-09 under 510(k) number K092335. The device is classified under product code BZH. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEAK EXPIRATORY FLOW METER, KN-9710?

PEAK EXPIRATORY FLOW METER, KN-9710 is a medical device that received FDA 510(k) clearance on 2010-04-09. The listed applicant is K-Jump Health Co., Ltd.. The 510(k) number is K092335.

When did PEAK EXPIRATORY FLOW METER, KN-9710 receive FDA 510(k) clearance?

PEAK EXPIRATORY FLOW METER, KN-9710 received FDA 510(k) clearance on 2010-04-09, under 510(k) number K092335.

Who is the listed applicant for PEAK EXPIRATORY FLOW METER, KN-9710?

The FDA 510(k) record lists K-Jump Health Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PEAK EXPIRATORY FLOW METER, KN-9710?

The FDA product code for PEAK EXPIRATORY FLOW METER, KN-9710 is BZH.

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 K-Jump Health Co., Ltd. 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.

K180714Probe Covers for ThermometersK170262Digital ThermometerK121520ULTRASONIC NEBULIZER (MESH TYPE)K120711NON-CONTACT THERMOMETERK103617DIGITAL FOREHEAD THERMOMETERK102947NON-CONTACT INFRARED THERMOMETER

View all 25 devices →

Related Devices (Code: BZH)

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.

K253180Microlife Digital Peak Flow Meter, Model PF200B (PF200B)Microlife CorporationK252802Peak Flow Meter (PF-10(BR-PEF231))Shenzhen Bi-Rich Medical Devices Co., Ltd.K241338Peak Flow MeterChongqing Moffy Innovation Technology Co., Ltd.K232588Aluna 2Knox Medical DiagnosticsK230423Electronic Peak Flow MeterTaian Dalu Medical Instrument Co., Ltd.K222810TD-7301 Peak Flow meterGostar Co., Ltd.

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.

↑