FDA 510(k)

MAXIMA FILTERED HARDSHELL RESERVIOR

K-Number: K933496 · 1993-10-15

Decision Date1993-10-15

Product CodeDTP

Advisory CommitteeCV

DecisionSubstantially Equivalent

Device Summary

MAXIMA FILTERED HARDSHELL RESERVIOR is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K933496. The device is classified under product code DTP. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MAXIMA FILTERED HARDSHELL RESERVIOR?

MAXIMA FILTERED HARDSHELL RESERVIOR is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Medtronic Vascular. The 510(k) number is K933496.

When did MAXIMA FILTERED HARDSHELL RESERVIOR receive FDA 510(k) clearance?

MAXIMA FILTERED HARDSHELL RESERVIOR received FDA 510(k) clearance on 1993-10-15, under 510(k) number K933496.

Who is the listed applicant for MAXIMA FILTERED HARDSHELL RESERVIOR?

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 MAXIMA FILTERED HARDSHELL RESERVIOR?

The FDA product code for MAXIMA FILTERED HARDSHELL RESERVIOR is DTP.

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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.