FDA 510(k)

COBRA SURGICAL PROBE

K-Number: K040219 · 2004-02-24

Decision Date2004-02-24

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

COBRA SURGICAL PROBE 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 2004-02-24 under 510(k) number K040219. 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 SURGICAL PROBE?

COBRA SURGICAL PROBE is a medical device that received FDA 510(k) clearance on 2004-02-24. The listed applicant is Boston Scientific Corp. The 510(k) number is K040219.

When did COBRA SURGICAL PROBE receive FDA 510(k) clearance?

COBRA SURGICAL PROBE received FDA 510(k) clearance on 2004-02-24, under 510(k) number K040219.

Who is the listed applicant for COBRA SURGICAL PROBE?

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 COBRA SURGICAL PROBE?

The FDA product code for COBRA SURGICAL PROBE is GEI.

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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.