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FDA 510(k)

RXPEAKFLOW

K-Number: K101380 · 2010-09-13

ApplicantNoble Marketing
Decision Date2010-09-13
Product CodeBZH
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RXPEAKFLOW is the device name listed in this FDA 510(k) record. The listed applicant is Noble Marketing. It received FDA 510(k) clearance on 2010-09-13 under 510(k) number K101380. 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 RXPEAKFLOW?

RXPEAKFLOW is a medical device that received FDA 510(k) clearance on 2010-09-13. The listed applicant is Noble Marketing. The 510(k) number is K101380.

When did RXPEAKFLOW receive FDA 510(k) clearance?

RXPEAKFLOW received FDA 510(k) clearance on 2010-09-13, under 510(k) number K101380.

Who is the listed applicant for RXPEAKFLOW?

The FDA 510(k) record lists Noble Marketing as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RXPEAKFLOW?

The FDA product code for RXPEAKFLOW is BZH.

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Other records listing Noble Marketing 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.

K110262SHARPS CONTAINER

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

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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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