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FDA 510(k)

NEO-I TEMPERATURE & CONDUCTIVITY METER

K-Number: K871708 · 1987-06-17

ApplicantAutomata, Inc.
Decision Date1987-06-17
Product CodeFIZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

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 1987-06-17 under 510(k) number K871708. 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 NEO-I TEMPERATURE & CONDUCTIVITY METER?

NEO-I TEMPERATURE & CONDUCTIVITY METER is a medical device that received FDA 510(k) clearance on 1987-06-17. The listed applicant is Automata, Inc.. The 510(k) number is K871708.

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

NEO-I TEMPERATURE & CONDUCTIVITY METER received FDA 510(k) clearance on 1987-06-17, under 510(k) number K871708.

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

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

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 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.

K881098MODIFIED NEO-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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