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FDA 510(k)

90XL INSTRUMENTATION SYSTEM

K-Number: K050812 · 2005-05-05

ApplicantMesa Laboratories, Inc.
Decision Date2005-05-05
Product CodeFIZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

90XL INSTRUMENTATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Mesa Laboratories, Inc.. It received FDA 510(k) clearance on 2005-05-05 under 510(k) number K050812. The device is classified under product code FIZ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 90XL INSTRUMENTATION SYSTEM?

90XL INSTRUMENTATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-05-05. The listed applicant is Mesa Laboratories, Inc.. The 510(k) number is K050812.

When did 90XL INSTRUMENTATION SYSTEM receive FDA 510(k) clearance?

90XL INSTRUMENTATION SYSTEM received FDA 510(k) clearance on 2005-05-05, under 510(k) number K050812.

Who is the listed applicant for 90XL INSTRUMENTATION SYSTEM?

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

What is the FDA product code for 90XL INSTRUMENTATION SYSTEM?

The FDA product code for 90XL INSTRUMENTATION SYSTEM is FIZ.

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Other records listing Mesa Laboratories, 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.

K201765SmartHDM-510 SystemK191496TDS Standard SolutionK130100COMINED STANDARD SOLUTIONK122362SMART-WELL INCUBATORK112018SMART READ EZTEST STEAMK033330CONDUCTIVITY/TDS CALIBRATOR SOLUTION

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Related Devices (Code: FIZ)

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.

K201765SmartHDM-510 SystemMesa Laboratories, Inc.K020909HDM99Ibp Instruments GmbHK020908HDM97Ibp Instruments GmbHK992431NEO-2 METERAutomata Instrumentation, Inc.K981294ODYSSEY INSTRUMENTATION SYSTEMAutomata Instrumentation, Inc.K955298PHOENIX DIALYSATE METERAutomata Medical Instrumentation, Inc.

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.

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