FDA 510(k)

ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES

K-Number: K946377 · 1995-03-24

Decision Date1995-03-24

Product CodeGEI

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Ximed Medical Systems. It received FDA 510(k) clearance on 1995-03-24 under 510(k) number K946377. 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 ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES?

ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES is a medical device that received FDA 510(k) clearance on 1995-03-24. The listed applicant is Ximed Medical Systems. The 510(k) number is K946377.

When did ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES receive FDA 510(k) clearance?

ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES received FDA 510(k) clearance on 1995-03-24, under 510(k) number K946377.

Who is the listed applicant for ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES?

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

What is the FDA product code for ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES?

The FDA product code for ELECTROPROBE SINGLE USE ELECTROSURGICAL PROBES is GEI.

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Other records listing Ximed Medical Systems as applicant

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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.