FDA 510(k)

MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD

K-Number: K873675 · 1987-10-06

Decision Date1987-10-06

Product CodeGZB

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD is the device name listed in this FDA 510(k) record. The listed applicant is Medtronic Vascular. It received FDA 510(k) clearance on 1987-10-06 under 510(k) number K873675. The device is classified under product code GZB. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD?

MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD is a medical device that received FDA 510(k) clearance on 1987-10-06. The listed applicant is Medtronic Vascular. The 510(k) number is K873675.

When did MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD receive FDA 510(k) clearance?

MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD received FDA 510(k) clearance on 1987-10-06, under 510(k) number K873675.

Who is the listed applicant for MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD?

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 MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD?

The FDA product code for MODIFIED #3587 RESUME SE-4/#3487 PISCES-QUAD is GZB.

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Official Source

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