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FDA 510(k)

DIGITAL MXR-D FLOWMETER

K-Number: K062155 · 2006-11-09

Decision Date2006-11-09
Product CodeBSZ
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

DIGITAL MXR-D FLOWMETER is the device name listed in this FDA 510(k) record. The listed applicant is Porter Instrument Co., Inc.. It received FDA 510(k) clearance on 2006-11-09 under 510(k) number K062155. The device is classified under product code BSZ. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITAL MXR-D FLOWMETER?

DIGITAL MXR-D FLOWMETER is a medical device that received FDA 510(k) clearance on 2006-11-09. The listed applicant is Porter Instrument Co., Inc.. The 510(k) number is K062155.

When did DIGITAL MXR-D FLOWMETER receive FDA 510(k) clearance?

DIGITAL MXR-D FLOWMETER received FDA 510(k) clearance on 2006-11-09, under 510(k) number K062155.

Who is the listed applicant for DIGITAL MXR-D FLOWMETER?

The FDA 510(k) record lists Porter Instrument Co., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DIGITAL MXR-D FLOWMETER?

The FDA product code for DIGITAL MXR-D FLOWMETER is BSZ.

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.

Other records listing Porter Instrument Co., Inc. 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.

Related Devices (Code: BSZ)

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.

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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