FDA 510(k)

MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE

K-Number: K901555 · 1990-07-18

Decision Date1990-07-18

Product CodeDRX

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1990-07-18 under 510(k) number K901555. The device is classified under product code DRX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE?

MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE is a medical device that received FDA 510(k) clearance on 1990-07-18. The listed applicant is Medtronic Vascular. The 510(k) number is K901555.

When did MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE receive FDA 510(k) clearance?

MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE received FDA 510(k) clearance on 1990-07-18, under 510(k) number K901555.

Who is the listed applicant for MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE?

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 MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE?

The FDA product code for MODEL 1730 NEOTRODE WITH ATTACHED LEADWIRE is DRX.

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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.