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FDA 510(k)

NEUROMED SELECTRA #7720

K-Number: K812704 · 1981-10-19

ApplicantMedtronic Vascular
Decision Date1981-10-19
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

NEUROMED SELECTRA #7720 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1981-10-19 under 510(k) number K812704. 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 SELECTRA #7720?

NEUROMED SELECTRA #7720 is a medical device that received FDA 510(k) clearance on 1981-10-19. The listed applicant is Medtronic Vascular. The 510(k) number is K812704.

When did NEUROMED SELECTRA #7720 receive FDA 510(k) clearance?

NEUROMED SELECTRA #7720 received FDA 510(k) clearance on 1981-10-19, under 510(k) number K812704.

Who is the listed applicant for NEUROMED SELECTRA #7720?

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

What is the FDA product code for NEUROMED SELECTRA #7720?

The FDA product code for NEUROMED SELECTRA #7720 is GZJ.

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Related Devices (Code: GZJ)

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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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