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FDA 510(k)

NEURO-CARE 1000

K-Number: K926265 · 1993-08-03

ApplicantEms Northwest
Decision Date1993-08-03
Product CodeIPF
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

NEURO-CARE 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Ems Northwest. It received FDA 510(k) clearance on 1993-08-03 under 510(k) number K926265. The device is classified under product code IPF. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEURO-CARE 1000?

NEURO-CARE 1000 is a medical device that received FDA 510(k) clearance on 1993-08-03. The listed applicant is Ems Northwest. The 510(k) number is K926265.

When did NEURO-CARE 1000 receive FDA 510(k) clearance?

NEURO-CARE 1000 received FDA 510(k) clearance on 1993-08-03, under 510(k) number K926265.

Who is the listed applicant for NEURO-CARE 1000?

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

What is the FDA product code for NEURO-CARE 1000?

The FDA product code for NEURO-CARE 1000 is IPF.

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Related Devices (Code: IPF)

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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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