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FDA 510(k)

COBRA BIPOLAR CLAMP, MODEL 15902

K-Number: K023288 · 2003-04-02

ApplicantBoston Scientific EP Technologies
Decision Date2003-04-02
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COBRA BIPOLAR CLAMP, MODEL 15902 is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific EP Technologies. It received FDA 510(k) clearance on 2003-04-02 under 510(k) number K023288. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COBRA BIPOLAR CLAMP, MODEL 15902?

COBRA BIPOLAR CLAMP, MODEL 15902 is a medical device that received FDA 510(k) clearance on 2003-04-02. The listed applicant is Boston Scientific EP Technologies. The 510(k) number is K023288.

When did COBRA BIPOLAR CLAMP, MODEL 15902 receive FDA 510(k) clearance?

COBRA BIPOLAR CLAMP, MODEL 15902 received FDA 510(k) clearance on 2003-04-02, under 510(k) number K023288.

Who is the listed applicant for COBRA BIPOLAR CLAMP, MODEL 15902?

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

What is the FDA product code for COBRA BIPOLAR CLAMP, MODEL 15902?

The FDA product code for COBRA BIPOLAR CLAMP, MODEL 15902 is GEI.

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Official Source

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