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FDA 510(k)

PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE

K-Number: K934023 · 1993-12-17

ApplicantPhx Technologies Corp.
Decision Date1993-12-17
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE 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 1993-12-17 under 510(k) number K934023. 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 PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE?

PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is Phx Technologies Corp.. The 510(k) number is K934023.

When did PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE receive FDA 510(k) clearance?

PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE received FDA 510(k) clearance on 1993-12-17, under 510(k) number K934023.

Who is the listed applicant for PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE?

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 PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE?

The FDA product code for PHX TECHNOLOGIES CORP., ALTRAUMATIC GRASPER DEVICE 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.

K262397CuratOR EX2742Eizo CorporationK260884UNIDRIVE Select SystemKarl Storz SE & CO. KGK260972OEV-271MUH LCD Monitor;OEV-321MUH LCD Monitor;OEV-431MUH LCD MonitorSony CorporationK261139VereSee (VER150, VER200, VER151, VER201, VER200C, and VER-100-103)Freyja Healthcare, LLCK253541EZ-Close™ (EZ Close Port Site Closing Device, EZ Close MAX Port Site Closing Device, EZ Close II Port Site Closing Device)Medical ImpactK261614LED LCD Monitor (OEV-271H)Lg Electronics.Inc

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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