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FDA 510(k)

ECLIPSE+, MODEL NUMBER 7723

K-Number: K865048 · 1987-02-26

ApplicantMedtronic Vascular
Decision Date1987-02-26
Product CodeGZJ
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

ECLIPSE+, MODEL NUMBER 7723 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-02-26 under 510(k) number K865048. 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 ECLIPSE+, MODEL NUMBER 7723?

ECLIPSE+, MODEL NUMBER 7723 is a medical device that received FDA 510(k) clearance on 1987-02-26. The listed applicant is Medtronic Vascular. The 510(k) number is K865048.

When did ECLIPSE+, MODEL NUMBER 7723 receive FDA 510(k) clearance?

ECLIPSE+, MODEL NUMBER 7723 received FDA 510(k) clearance on 1987-02-26, under 510(k) number K865048.

Who is the listed applicant for ECLIPSE+, MODEL NUMBER 7723?

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 ECLIPSE+, MODEL NUMBER 7723?

The FDA product code for ECLIPSE+, MODEL NUMBER 7723 is GZJ.

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Related Devices (Code: GZJ)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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