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FDA 510(k)

CAUTERY TIP CLEANER, MODEL 30500

K-Number: K053433 · 2006-01-19

ApplicantXodus Medical, Inc.
Decision Date2006-01-19
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CAUTERY TIP CLEANER, MODEL 30500 is the device name listed in this FDA 510(k) record. The listed applicant is Xodus Medical, Inc.. It received FDA 510(k) clearance on 2006-01-19 under 510(k) number K053433. 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 CAUTERY TIP CLEANER, MODEL 30500?

CAUTERY TIP CLEANER, MODEL 30500 is a medical device that received FDA 510(k) clearance on 2006-01-19. The listed applicant is Xodus Medical, Inc.. The 510(k) number is K053433.

When did CAUTERY TIP CLEANER, MODEL 30500 receive FDA 510(k) clearance?

CAUTERY TIP CLEANER, MODEL 30500 received FDA 510(k) clearance on 2006-01-19, under 510(k) number K053433.

Who is the listed applicant for CAUTERY TIP CLEANER, MODEL 30500?

The FDA 510(k) record lists Xodus Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CAUTERY TIP CLEANER, MODEL 30500?

The FDA product code for CAUTERY TIP CLEANER, MODEL 30500 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.

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