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FDA 510(k)

INSUFFLATION TUBING SET, PHX500-082

K-Number: K935059 · 1993-12-22

ApplicantPhx Technologies Corp.
Decision Date1993-12-22
Product CodeFCX
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

INSUFFLATION TUBING SET, PHX500-082 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 1993-12-22 under 510(k) number K935059. The device is classified under product code FCX. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSUFFLATION TUBING SET, PHX500-082?

INSUFFLATION TUBING SET, PHX500-082 is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Phx Technologies Corp.. The 510(k) number is K935059.

When did INSUFFLATION TUBING SET, PHX500-082 receive FDA 510(k) clearance?

INSUFFLATION TUBING SET, PHX500-082 received FDA 510(k) clearance on 1993-12-22, under 510(k) number K935059.

Who is the listed applicant for INSUFFLATION TUBING SET, PHX500-082?

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 INSUFFLATION TUBING SET, PHX500-082?

The FDA product code for INSUFFLATION TUBING SET, PHX500-082 is FCX.

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Other records listing Phx Technologies Corp. as applicant

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Related Devices (Code: FCX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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