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FDA 510(k)

EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER

K-Number: K874850 · 1988-05-20

ApplicantEpi-Scan Corp.
Decision Date1988-05-20
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is Epi-Scan Corp.. It received FDA 510(k) clearance on 1988-05-20 under 510(k) number K874850. The device is classified under product code GZO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER?

EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER is a medical device that received FDA 510(k) clearance on 1988-05-20. The listed applicant is Epi-Scan Corp.. The 510(k) number is K874850.

When did EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER receive FDA 510(k) clearance?

EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER received FDA 510(k) clearance on 1988-05-20, under 510(k) number K874850.

Who is the listed applicant for EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER?

The FDA 510(k) record lists Epi-Scan Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER?

The FDA product code for EPI-SCAN SELECTIVE TISSUE CONDUCTANCE METER is GZO.

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Related Devices (Code: GZO)

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.

K131568SUDO PATHLd Technology, LLCK111308ZYTO HAND CRADLEZyto Technologies, Inc.K102166ELECTRO INTERSTITIAL SCANLd Technology, LLCK100233SUDOSCANImpeto MedicalK053004MSAS-VANTAGEBiomeridian, Int.K032935EPI-SCAN, MODEL P 100Edx Epi-Scan, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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