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FDA 510(k)

POREX NERVE LOCATOR

K-Number: K872791 · 1987-10-20

ApplicantPorex Medical
Decision Date1987-10-20
Product CodeETN
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

POREX NERVE LOCATOR is the device name listed in this FDA 510(k) record. The listed applicant is Porex Medical. It received FDA 510(k) clearance on 1987-10-20 under 510(k) number K872791. The device is classified under product code ETN. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the POREX NERVE LOCATOR?

POREX NERVE LOCATOR is a medical device that received FDA 510(k) clearance on 1987-10-20. The listed applicant is Porex Medical. The 510(k) number is K872791.

When did POREX NERVE LOCATOR receive FDA 510(k) clearance?

POREX NERVE LOCATOR received FDA 510(k) clearance on 1987-10-20, under 510(k) number K872791.

Who is the listed applicant for POREX NERVE LOCATOR?

The FDA 510(k) record lists Porex Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for POREX NERVE LOCATOR?

The FDA product code for POREX NERVE LOCATOR is ETN.

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Other records listing Porex Medical as applicant

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.

K873044POREX OTOLOGY INSTRUMENTSK872947POREX QUALITY PLASTIC SURGERY INSTRUMENTSK863946POREX(TM) EXTRA-OCULAR ORBITAL IMPLANTK863943POREX(TM) EYE SPHERE IMPLANTK870257POREX(TM) SILICONE SURGICAL IMPLANTS FOR E.N.T.K870154POREX(TM) TISSUE EXPANDER

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Related Devices (Code: ETN)

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.

K253536Evala Nerve Stimulator (EPNR002)Epineuron Technologies, Inc.K251672NIM Essence™ EMG Endotracheal Tube (NIMEID060); NIM Essence™ EMG Endotracheal Tube (NIMEID065); NIM Essence™ EMG Endotracheal Tube (NIMEID070); NIM Essence™ EMG Endotracheal Tube (NIMEID075); NIM Essence™ EMG Endotracheal Tube (NIMEID080)Medtronic Xomed, Inc.K242852ALM Tube I.D. 6.0, O.D. 8.2 (520843), ALM Tube I.D. 7.0, O.D. 9.7 (520845), ALM Tube I.D. 7.5, O.D. 10.3 (520846), ALM Tube I.D. 8.0, O.D. 11.0 (520847)Inomed Medizintechnik GmbHK233001Bioscope Neuromonitor DeviceBiosys Biyomedikal Muhendislik San. VE Tic. A.S.K241917EARP Nerve Cuff ElectrodeRetropsoas Technologies, LLCK232888Disposable Laryngeal ElectrodesSuzhou Haishen Medical Device Associates Co., Ltd.

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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