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FDA 510(k)

DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR

K-Number: K020400 · 2002-08-23

ApplicantMeps, LLC
Decision Date2002-08-23
Product CodeGWF
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR is the device name listed in this FDA 510(k) record. The listed applicant is Meps, LLC. It received FDA 510(k) clearance on 2002-08-23 under 510(k) number K020400. The device is classified under product code GWF. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR?

DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR is a medical device that received FDA 510(k) clearance on 2002-08-23. The listed applicant is Meps, LLC. The 510(k) number is K020400.

When did DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR receive FDA 510(k) clearance?

DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR received FDA 510(k) clearance on 2002-08-23, under 510(k) number K020400.

Who is the listed applicant for DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR?

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

What is the FDA product code for DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR?

The FDA product code for DIGITIMER D185 MULTIPULSE CORTICAL STIMULATOR is GWF.

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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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