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FDA 510(k)

GALVANIC SKIN RESPONSE DEVICE

K-Number: K943101 · 1995-10-18

ApplicantGlobal Ent.
Decision Date1995-10-18
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

GALVANIC SKIN RESPONSE DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Global Ent.. It received FDA 510(k) clearance on 1995-10-18 under 510(k) number K943101. 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 GALVANIC SKIN RESPONSE DEVICE?

GALVANIC SKIN RESPONSE DEVICE is a medical device that received FDA 510(k) clearance on 1995-10-18. The listed applicant is Global Ent.. The 510(k) number is K943101.

When did GALVANIC SKIN RESPONSE DEVICE receive FDA 510(k) clearance?

GALVANIC SKIN RESPONSE DEVICE received FDA 510(k) clearance on 1995-10-18, under 510(k) number K943101.

Who is the listed applicant for GALVANIC SKIN RESPONSE DEVICE?

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

What is the FDA product code for GALVANIC SKIN RESPONSE DEVICE?

The FDA product code for GALVANIC SKIN RESPONSE DEVICE is GZO.

Related Clinical Trials

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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

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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