FDA 510(k)

PERCUPASS TUNNELING TOOL MODEL 3452

K-Number: K772013 · 1977-10-28

Decision Date1977-10-28

Product CodeHAO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

PERCUPASS TUNNELING TOOL MODEL 3452 is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1977-10-28 under 510(k) number K772013. The device is classified under product code HAO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERCUPASS TUNNELING TOOL MODEL 3452?

PERCUPASS TUNNELING TOOL MODEL 3452 is a medical device that received FDA 510(k) clearance on 1977-10-28. The listed applicant is Medtronic Vascular. The 510(k) number is K772013.

When did PERCUPASS TUNNELING TOOL MODEL 3452 receive FDA 510(k) clearance?

PERCUPASS TUNNELING TOOL MODEL 3452 received FDA 510(k) clearance on 1977-10-28, under 510(k) number K772013.

Who is the listed applicant for PERCUPASS TUNNELING TOOL MODEL 3452?

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 PERCUPASS TUNNELING TOOL MODEL 3452?

The FDA product code for PERCUPASS TUNNELING TOOL MODEL 3452 is HAO.

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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.