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FDA 510(k)

PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES

K-Number: K932392 · 1993-11-22

ApplicantPhx Technologies Corp.
Decision Date1993-11-22
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES is the device name listed in this FDA 510(k) record. The listed applicant is Phx Technologies Corp.. It received FDA 510(k) clearance on 1993-11-22 under 510(k) number K932392. 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 PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES?

PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES is a medical device that received FDA 510(k) clearance on 1993-11-22. The listed applicant is Phx Technologies Corp.. The 510(k) number is K932392.

When did PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES receive FDA 510(k) clearance?

PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES received FDA 510(k) clearance on 1993-11-22, under 510(k) number K932392.

Who is the listed applicant for PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES?

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

What is the FDA product code for PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES?

The FDA product code for PHX TECHNOLOGIES CORP ELECTROSURGICAL PROBES is GEI.

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Other records listing Phx Technologies Corp. as applicant

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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