FDA 510(k)

CONTOUR SE MICROSPHERES

K-Number: K022427 · 2002-08-22

Decision Date2002-08-22

Product CodeHCG

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

CONTOUR SE MICROSPHERES is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 2002-08-22 under 510(k) number K022427. The device is classified under product code HCG. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONTOUR SE MICROSPHERES?

CONTOUR SE MICROSPHERES is a medical device that received FDA 510(k) clearance on 2002-08-22. The listed applicant is Boston Scientific Corp. The 510(k) number is K022427.

When did CONTOUR SE MICROSPHERES receive FDA 510(k) clearance?

CONTOUR SE MICROSPHERES received FDA 510(k) clearance on 2002-08-22, under 510(k) number K022427.

Who is the listed applicant for CONTOUR SE MICROSPHERES?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CONTOUR SE MICROSPHERES?

The FDA product code for CONTOUR SE MICROSPHERES is HCG.

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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.