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FDA 510(k)

NEUROCOM PRESSURE TEST SYSTEM

K-Number: K871652 · 1987-07-16

ApplicantNeurocom International, Inc.
Decision Date1987-07-16
Product CodeETY
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

NEUROCOM PRESSURE TEST SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Neurocom International, Inc.. It received FDA 510(k) clearance on 1987-07-16 under 510(k) number K871652. The device is classified under product code ETY. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROCOM PRESSURE TEST SYSTEM?

NEUROCOM PRESSURE TEST SYSTEM is a medical device that received FDA 510(k) clearance on 1987-07-16. The listed applicant is Neurocom International, Inc.. The 510(k) number is K871652.

When did NEUROCOM PRESSURE TEST SYSTEM receive FDA 510(k) clearance?

NEUROCOM PRESSURE TEST SYSTEM received FDA 510(k) clearance on 1987-07-16, under 510(k) number K871652.

Who is the listed applicant for NEUROCOM PRESSURE TEST SYSTEM?

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

What is the FDA product code for NEUROCOM PRESSURE TEST SYSTEM?

The FDA product code for NEUROCOM PRESSURE TEST SYSTEM is ETY.

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Other records listing Neurocom International, 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.

K946229BALANCE MANAGERK901732EMG ACCESSORY FOR POSTUROGRAPHYK863443DUAL FORCEPLATEK851744EQUITEST

Related Devices (Code: ETY)

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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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