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FDA 510(k)

EEC PROBE

K-Number: K935115 · 1994-03-11

ApplicantPhx Technologies Corp.
Decision Date1994-03-11
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

EEC PROBE 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 1994-03-11 under 510(k) number K935115. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EEC PROBE?

EEC PROBE is a medical device that received FDA 510(k) clearance on 1994-03-11. The listed applicant is Phx Technologies Corp.. The 510(k) number is K935115.

When did EEC PROBE receive FDA 510(k) clearance?

EEC PROBE received FDA 510(k) clearance on 1994-03-11, under 510(k) number K935115.

Who is the listed applicant for EEC PROBE?

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 EEC PROBE?

The FDA product code for EEC PROBE is GCJ.

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Related Devices (Code: GCJ)

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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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