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FDA 510(k)

NMI SOFTWARE

K-Number: K950270 · 1995-05-15

ApplicantNicolet Biomedical, Inc.
Decision Date1995-05-15
Product CodeOMB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NMI SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Nicolet Biomedical, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K950270. The device is classified under product code OMB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NMI SOFTWARE?

NMI SOFTWARE is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is Nicolet Biomedical, Inc.. The 510(k) number is K950270.

When did NMI SOFTWARE receive FDA 510(k) clearance?

NMI SOFTWARE received FDA 510(k) clearance on 1995-05-15, under 510(k) number K950270.

Who is the listed applicant for NMI SOFTWARE?

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

What is the FDA product code for NMI SOFTWARE?

The FDA product code for NMI SOFTWARE is OMB.

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Other records listing Nicolet Biomedical, Inc. as applicant

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Related Devices (Code: OMB)

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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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