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FDA 510(k)

NERVUS MONITOR

K-Number: K021185 · 2002-07-12

ApplicantTaugagreining HF
Decision Date2002-07-12
Product CodeOLV
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NERVUS MONITOR is the device name listed in this FDA 510(k) record. The listed applicant is Taugagreining HF. It received FDA 510(k) clearance on 2002-07-12 under 510(k) number K021185. The device is classified under product code OLV. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NERVUS MONITOR?

NERVUS MONITOR is a medical device that received FDA 510(k) clearance on 2002-07-12. The listed applicant is Taugagreining HF. The 510(k) number is K021185.

When did NERVUS MONITOR receive FDA 510(k) clearance?

NERVUS MONITOR received FDA 510(k) clearance on 2002-07-12, under 510(k) number K021185.

Who is the listed applicant for NERVUS MONITOR?

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

What is the FDA product code for NERVUS MONITOR?

The FDA product code for NERVUS MONITOR is OLV.

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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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