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FDA 510(k)

NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS

K-Number: K083250 · 2009-08-18

ApplicantAa Neuromed Corp.
Decision Date2009-08-18
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Aa Neuromed Corp.. It received FDA 510(k) clearance on 2009-08-18 under 510(k) number K083250. The device is classified under product code GZJ. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS?

NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS is a medical device that received FDA 510(k) clearance on 2009-08-18. The listed applicant is Aa Neuromed Corp.. The 510(k) number is K083250.

When did NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS receive FDA 510(k) clearance?

NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS received FDA 510(k) clearance on 2009-08-18, under 510(k) number K083250.

Who is the listed applicant for NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS?

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

What is the FDA product code for NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS?

The FDA product code for NEUROMED ELECTROANALGESIC DELIVERY SYSTEMS is GZJ.

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Related Devices (Code: GZJ)

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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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