FDA 510(k)

INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER

K-Number: K110887 · 2011-04-14

Decision Date2011-04-14

Product CodeKNS

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2011-04-14 under 510(k) number K110887. The device is classified under product code KNS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER?

INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER is a medical device that received FDA 510(k) clearance on 2011-04-14. The listed applicant is Boston Scientific Corporation. The 510(k) number is K110887.

When did INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER receive FDA 510(k) clearance?

INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER received FDA 510(k) clearance on 2011-04-14, under 510(k) number K110887.

Who is the listed applicant for INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER?

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

What is the FDA product code for INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER?

The FDA product code for INJECTION GOLD PROBE BIPOLAR ELECTROHEMOSTASIS CATHETER is KNS.

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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.