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FDA 510(k)

RAPID PROGRAMMAR

K-Number: K030118 · 2003-03-11

ApplicantAdvanced Neuromodulation Systems
Decision Date2003-03-11
Product CodeGZB
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RAPID PROGRAMMAR is the device name listed in this FDA 510(k) record. The listed applicant is Advanced Neuromodulation Systems. It received FDA 510(k) clearance on 2003-03-11 under 510(k) number K030118. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RAPID PROGRAMMAR?

RAPID PROGRAMMAR is a medical device that received FDA 510(k) clearance on 2003-03-11. The listed applicant is Advanced Neuromodulation Systems. The 510(k) number is K030118.

When did RAPID PROGRAMMAR receive FDA 510(k) clearance?

RAPID PROGRAMMAR received FDA 510(k) clearance on 2003-03-11, under 510(k) number K030118.

Who is the listed applicant for RAPID PROGRAMMAR?

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

What is the FDA product code for RAPID PROGRAMMAR?

The FDA product code for RAPID PROGRAMMAR is GZB.

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Other records listing Advanced Neuromodulation Systems as applicant

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Related Devices (Code: GZB)

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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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