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FDA 510(k)

SMARTFLOW PULSE TRANSMISSION COEFFICIENT

K-Number: K020127 · 2002-02-14

ApplicantFlorence Medical , Ltd.
Decision Date2002-02-14
Product CodeDQK
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SMARTFLOW PULSE TRANSMISSION COEFFICIENT is the device name listed in this FDA 510(k) record. The listed applicant is Florence Medical , Ltd.. It received FDA 510(k) clearance on 2002-02-14 under 510(k) number K020127. The device is classified under product code DQK. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMARTFLOW PULSE TRANSMISSION COEFFICIENT?

SMARTFLOW PULSE TRANSMISSION COEFFICIENT is a medical device that received FDA 510(k) clearance on 2002-02-14. The listed applicant is Florence Medical , Ltd.. The 510(k) number is K020127.

When did SMARTFLOW PULSE TRANSMISSION COEFFICIENT receive FDA 510(k) clearance?

SMARTFLOW PULSE TRANSMISSION COEFFICIENT received FDA 510(k) clearance on 2002-02-14, under 510(k) number K020127.

Who is the listed applicant for SMARTFLOW PULSE TRANSMISSION COEFFICIENT?

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

What is the FDA product code for SMARTFLOW PULSE TRANSMISSION COEFFICIENT?

The FDA product code for SMARTFLOW PULSE TRANSMISSION COEFFICIENT is DQK.

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.

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Other records listing Florence Medical , 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.

K012947SMARTFLOWK003122SMARTFLOW, MODEL SFIP 2000

Related Devices (Code: DQK)

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.

K261729EnSite™ X EP SystemAbbott MedicalK262005Affera Integrated Mapping SystemMedtronic, Inc.K253692AVVIGO™+ Multi-Modality Guidance SystemBoston ScientificK253576CorVista System® with PCWP Add-OnAnalytics For Life, Inc.K262006EnSite™ X EP SystemAbbott MedicalK252978ScioCardio ECG Analysis PlatformSynergen Technology Labs, LLC

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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