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)

VM PLUS PEAK FLOWMETER

K-Number: K962074 · 1997-01-02

ApplicantClement Clarke Intl., Ltd.
Decision Date1997-01-02
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

VM PLUS PEAK FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Clement Clarke Intl., Ltd.. It received FDA 510(k) clearance on 1997-01-02 under 510(k) number K962074. 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 VM PLUS PEAK FLOWMETER?

VM PLUS PEAK FLOWMETER is a medical device that received FDA 510(k) clearance on 1997-01-02. The listed applicant is Clement Clarke Intl., Ltd.. The 510(k) number is K962074.

When did VM PLUS PEAK FLOWMETER receive FDA 510(k) clearance?

VM PLUS PEAK FLOWMETER received FDA 510(k) clearance on 1997-01-02, under 510(k) number K962074.

Who is the listed applicant for VM PLUS PEAK FLOWMETER?

The FDA 510(k) record lists Clement Clarke Intl., Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VM PLUS PEAK FLOWMETER?

The FDA product code for VM PLUS PEAK FLOWMETER 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 Clement Clarke Intl., 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.

K053156MINI-WRIGHT DIGITAL, MODEL 3120001K042058ONEFLOW FVC, ONEFLOW FVC (KIT), ONEFLOW FVC SCREENK000368EYECAP IMAGING SYSTEMK982334AIRZONE PEAK FLOWMETERK980960IN-CHECK INSPIRATORY FLOWMETER

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.

↑