FDA 510(k)

SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64

K-Number: K090267 · 2009-03-16

Decision Date2009-03-16

Product CodeMOS

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 is the device name listed in this FDA 510(k) record. The listed applicant is Midwest Rf, LLC. It received FDA 510(k) clearance on 2009-03-16 under 510(k) number K090267. The device is classified under product code MOS. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64?

SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 is a medical device that received FDA 510(k) clearance on 2009-03-16. The listed applicant is Midwest Rf, LLC. The 510(k) number is K090267.

When did SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 receive FDA 510(k) clearance?

SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 received FDA 510(k) clearance on 2009-03-16, under 510(k) number K090267.

Who is the listed applicant for SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64?

The FDA 510(k) record lists Midwest Rf, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64?

The FDA product code for SV DBS BRAIN ARRAY, MODEL 1500SV-SMS64 is MOS.

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Other records listing Midwest Rf, LLC as applicant

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Related Devices (Code: MOS)

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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.