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FDA 510(k)

5MM CALIBRATED SUCTION CANNULA

K-Number: K934158 · 1994-01-26

ApplicantPhx Technologies Corp.
Decision Date1994-01-26
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

5MM CALIBRATED SUCTION CANNULA 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 1994-01-26 under 510(k) number K934158. 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 5MM CALIBRATED SUCTION CANNULA?

5MM CALIBRATED SUCTION CANNULA is a medical device that received FDA 510(k) clearance on 1994-01-26. The listed applicant is Phx Technologies Corp.. The 510(k) number is K934158.

When did 5MM CALIBRATED SUCTION CANNULA receive FDA 510(k) clearance?

5MM CALIBRATED SUCTION CANNULA received FDA 510(k) clearance on 1994-01-26, under 510(k) number K934158.

Who is the listed applicant for 5MM CALIBRATED SUCTION CANNULA?

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 5MM CALIBRATED SUCTION CANNULA?

The FDA product code for 5MM CALIBRATED SUCTION CANNULA is GCJ.

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Other records listing Phx Technologies Corp. as applicant

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Related Devices (Code: GCJ)

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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