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FDA 510(k)

MAXMIXING BLOCK

K-Number: K113232 · 2012-03-01

ApplicantMaxtec, Inc.
Decision Date2012-03-01
Product CodeBZR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MAXMIXING BLOCK is the device name listed in this FDA 510(k) record. The listed applicant is Maxtec, Inc.. It received FDA 510(k) clearance on 2012-03-01 under 510(k) number K113232. The device is classified under product code BZR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXMIXING BLOCK?

MAXMIXING BLOCK is a medical device that received FDA 510(k) clearance on 2012-03-01. The listed applicant is Maxtec, Inc.. The 510(k) number is K113232.

When did MAXMIXING BLOCK receive FDA 510(k) clearance?

MAXMIXING BLOCK received FDA 510(k) clearance on 2012-03-01, under 510(k) number K113232.

Who is the listed applicant for MAXMIXING BLOCK?

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

What is the FDA product code for MAXMIXING BLOCK?

The FDA product code for MAXMIXING BLOCK is BZR.

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 Maxtec, 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.

K063488MAXO2 CUK040484MAXO2+, MODEL A AND AE

Related Devices (Code: BZR)

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.

K243917F&P Optiflow Air/Oxygen Flow SourceFisher & Paykel Healthcare, Ltd.K241465Midas Flowmeter; eAVSParker Hannifin CorporationK231895Maxtec MaxBlend2+pMaxtec, LLCK230987FlowStar Analog Mixer FlowmeterBaldus Sedation GmbH & Co. KGK222794FlowStar Touch Digital Mixer FlowmeterBaldus Sedation GmbH & Co. KGK221494Quality Mix Blender, OxymixerDehas Medical Systems GmbH

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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