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)

IN-CHECK INSPIRATORY FLOWMETER

K-Number: K980960 · 1998-06-10

ApplicantClement Clarke Intl., Ltd.
Decision Date1998-06-10
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IN-CHECK INSPIRATORY 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 1998-06-10 under 510(k) number K980960. 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 IN-CHECK INSPIRATORY FLOWMETER?

IN-CHECK INSPIRATORY FLOWMETER is a medical device that received FDA 510(k) clearance on 1998-06-10. The listed applicant is Clement Clarke Intl., Ltd.. The 510(k) number is K980960.

When did IN-CHECK INSPIRATORY FLOWMETER receive FDA 510(k) clearance?

IN-CHECK INSPIRATORY FLOWMETER received FDA 510(k) clearance on 1998-06-10, under 510(k) number K980960.

Who is the listed applicant for IN-CHECK INSPIRATORY 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 IN-CHECK INSPIRATORY FLOWMETER?

The FDA product code for IN-CHECK INSPIRATORY 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 FLOWMETERK962074VM PLUS PEAK 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.

↑