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FDA 510(k)

MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT

K-Number: K780932 · 1978-08-31

ApplicantWestern Laboratories Corp.
Decision Date1978-08-31
Product CodeFIZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT is the device name listed in this FDA 510(k) record. The listed applicant is Western Laboratories Corp.. It received FDA 510(k) clearance on 1978-08-31 under 510(k) number K780932. 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 MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT?

MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT is a medical device that received FDA 510(k) clearance on 1978-08-31. The listed applicant is Western Laboratories Corp.. The 510(k) number is K780932.

When did MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT receive FDA 510(k) clearance?

MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT received FDA 510(k) clearance on 1978-08-31, under 510(k) number K780932.

Who is the listed applicant for MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT?

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

What is the FDA product code for MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT?

The FDA product code for MODEL 80 CONDUCTIVITY/TEMP.TEST UNIT is FIZ.

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Other records listing Western Laboratories Corp. 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.

K834024HEPARINOMETERK830468MODEL 200K821834MODEL 100 BICARBONATE CONDUCTIVITYK821415MODEL 90 BCK821414MODEL 80 BCK801303MODEL 90 PRESSURE/CONDUCTIVITY/TEMP TEST

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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.K05081290XL INSTRUMENTATION SYSTEMMesa Laboratories, Inc.K020908HDM97Ibp Instruments GmbHK020909HDM99Ibp Instruments GmbHK992431NEO-2 METERAutomata Instrumentation, Inc.K981294ODYSSEY INSTRUMENTATION SYSTEMAutomata 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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