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FDA 510(k)

MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER

K-Number: K881098 · 1988-04-21

ApplicantAutomata, Inc.
Decision Date1988-04-21
Product CodeFIZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER is the device name listed in this FDA 510(k) record. The listed applicant is Automata, Inc.. It received FDA 510(k) clearance on 1988-04-21 under 510(k) number K881098. 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 MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER?

MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER is a medical device that received FDA 510(k) clearance on 1988-04-21. The listed applicant is Automata, Inc.. The 510(k) number is K881098.

When did MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER receive FDA 510(k) clearance?

MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER received FDA 510(k) clearance on 1988-04-21, under 510(k) number K881098.

Who is the listed applicant for MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER?

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

What is the FDA product code for MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER?

The FDA product code for MODIFIED NEO-I TEMPERATURE, CONDUCTIVITY METER is FIZ.

Related Clinical Trials

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Other records listing Automata, 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.

K871708NEO-I TEMPERATURE & CONDUCTIVITY METER

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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