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FDA 510(k)

CARPAL TUNNEL SLOTTED CANNULA

K-Number: K954464 · 1995-10-23

ApplicantPhx Technologies Corp.
Decision Date1995-10-23
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CARPAL TUNNEL SLOTTED 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 1995-10-23 under 510(k) number K954464. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARPAL TUNNEL SLOTTED CANNULA?

CARPAL TUNNEL SLOTTED CANNULA is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is Phx Technologies Corp.. The 510(k) number is K954464.

When did CARPAL TUNNEL SLOTTED CANNULA receive FDA 510(k) clearance?

CARPAL TUNNEL SLOTTED CANNULA received FDA 510(k) clearance on 1995-10-23, under 510(k) number K954464.

Who is the listed applicant for CARPAL TUNNEL SLOTTED 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 CARPAL TUNNEL SLOTTED CANNULA?

The FDA product code for CARPAL TUNNEL SLOTTED CANNULA is HRX.

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Other records listing Phx Technologies Corp. as applicant

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Related Devices (Code: HRX)

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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