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FDA 510(k)

NEO-2 METER

K-Number: K992431 · 1999-10-13

ApplicantAutomata Instrumentation, Inc.
Decision Date1999-10-13
Product CodeFIZ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NEO-2 METER is the device name listed in this FDA 510(k) record. The listed applicant is Automata Instrumentation, Inc.. It received FDA 510(k) clearance on 1999-10-13 under 510(k) number K992431. 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-2 METER?

NEO-2 METER is a medical device that received FDA 510(k) clearance on 1999-10-13. The listed applicant is Automata Instrumentation, Inc.. The 510(k) number is K992431.

When did NEO-2 METER receive FDA 510(k) clearance?

NEO-2 METER received FDA 510(k) clearance on 1999-10-13, under 510(k) number K992431.

Who is the listed applicant for NEO-2 METER?

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

What is the FDA product code for NEO-2 METER?

The FDA product code for NEO-2 METER is FIZ.

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Other records listing Automata Instrumentation, 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.

K981294ODYSSEY INSTRUMENTATION SYSTEMK974127HYDRA 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 GmbHK981294ODYSSEY INSTRUMENTATION SYSTEMAutomata Instrumentation, Inc.K955298PHOENIX DIALYSATE METERAutomata Medical Instrumentation, Inc.

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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