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FDA 510(k)

WATTS RAKE WITH LEUR LOCK PORT

K-Number: K934153 · 1994-03-18

ApplicantPhx Technologies Corp.
Decision Date1994-03-18
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

WATTS RAKE WITH LEUR LOCK PORT 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 1994-03-18 under 510(k) number K934153. 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 WATTS RAKE WITH LEUR LOCK PORT?

WATTS RAKE WITH LEUR LOCK PORT is a medical device that received FDA 510(k) clearance on 1994-03-18. The listed applicant is Phx Technologies Corp.. The 510(k) number is K934153.

When did WATTS RAKE WITH LEUR LOCK PORT receive FDA 510(k) clearance?

WATTS RAKE WITH LEUR LOCK PORT received FDA 510(k) clearance on 1994-03-18, under 510(k) number K934153.

Who is the listed applicant for WATTS RAKE WITH LEUR LOCK PORT?

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 WATTS RAKE WITH LEUR LOCK PORT?

The FDA product code for WATTS RAKE WITH LEUR LOCK PORT 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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