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FDA 510(k)

BRAVO MULTI-MODALITY SYSTEM

K-Number: K991054 · 1999-11-03

ApplicantNicolet Biomedical, Inc.
Decision Date1999-11-03
Product CodeGWQ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

BRAVO MULTI-MODALITY SYSTEM 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 1999-11-03 under 510(k) number K991054. The device is classified under product code GWQ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRAVO MULTI-MODALITY SYSTEM?

BRAVO MULTI-MODALITY SYSTEM is a medical device that received FDA 510(k) clearance on 1999-11-03. The listed applicant is Nicolet Biomedical, Inc.. The 510(k) number is K991054.

When did BRAVO MULTI-MODALITY SYSTEM receive FDA 510(k) clearance?

BRAVO MULTI-MODALITY SYSTEM received FDA 510(k) clearance on 1999-11-03, under 510(k) number K991054.

Who is the listed applicant for BRAVO MULTI-MODALITY SYSTEM?

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 BRAVO MULTI-MODALITY SYSTEM?

The FDA product code for BRAVO MULTI-MODALITY SYSTEM is GWQ.

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Other records listing Nicolet Biomedical, Inc. as applicant

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Related Devices (Code: GWQ)

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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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