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FDA 510(k)

SDR (SOFT DISSECTOR RAKE)

K-Number: K935109 · 1994-03-21

ApplicantPhx Technologies Corp.
Decision Date1994-03-21
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SDR (SOFT DISSECTOR RAKE) 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 1994-03-21 under 510(k) number K935109. 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 SDR (SOFT DISSECTOR RAKE)?

SDR (SOFT DISSECTOR RAKE) is a medical device that received FDA 510(k) clearance on 1994-03-21. The listed applicant is Phx Technologies Corp.. The 510(k) number is K935109.

When did SDR (SOFT DISSECTOR RAKE) receive FDA 510(k) clearance?

SDR (SOFT DISSECTOR RAKE) received FDA 510(k) clearance on 1994-03-21, under 510(k) number K935109.

Who is the listed applicant for SDR (SOFT DISSECTOR RAKE)?

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 SDR (SOFT DISSECTOR RAKE)?

The FDA product code for SDR (SOFT DISSECTOR RAKE) 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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