FDA 510(k)

INTERSEPT 1375 VENOUS RESERVOIR

K-Number: K903632 · 1990-12-17

Decision Date1990-12-17

Product CodeDTN

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

INTERSEPT 1375 VENOUS RESERVOIR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1990-12-17 under 510(k) number K903632. The device is classified under product code DTN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTERSEPT 1375 VENOUS RESERVOIR?

INTERSEPT 1375 VENOUS RESERVOIR is a medical device that received FDA 510(k) clearance on 1990-12-17. The listed applicant is Medtronic Vascular. The 510(k) number is K903632.

When did INTERSEPT 1375 VENOUS RESERVOIR receive FDA 510(k) clearance?

INTERSEPT 1375 VENOUS RESERVOIR received FDA 510(k) clearance on 1990-12-17, under 510(k) number K903632.

Who is the listed applicant for INTERSEPT 1375 VENOUS RESERVOIR?

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 INTERSEPT 1375 VENOUS RESERVOIR?

The FDA product code for INTERSEPT 1375 VENOUS RESERVOIR is DTN.

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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.