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FDA 510(k)

MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES

K-Number: K923407 · 1992-10-19

Decision Date1992-10-19
Product CodeLDF
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1992-10-19 under 510(k) number K923407. The device is classified under product code LDF. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES?

MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES is a medical device that received FDA 510(k) clearance on 1992-10-19. The listed applicant is Medtronic Vascular. The 510(k) number is K923407.

When did MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES receive FDA 510(k) clearance?

MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES received FDA 510(k) clearance on 1992-10-19, under 510(k) number K923407.

Who is the listed applicant for MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES?

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 MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES?

The FDA product code for MEDTRONIC MODELS 5455L AND 5455SL SURGICAL CABLES is LDF.

Related Clinical Trials

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.

Other records listing Medtronic Vascular as applicant

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.

View all 474 devices →

Related Devices (Code: LDF)

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.

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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