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FDA 510(k)

DERMATRON SKIN RESISTANCE METER

K-Number: K883112 · 1989-08-10

ApplicantRaymar Electronics
Decision Date1989-08-10
Product CodeGZO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

DERMATRON SKIN RESISTANCE METER is the device name listed in this FDA 510(k) record. The listed applicant is Raymar Electronics. It received FDA 510(k) clearance on 1989-08-10 under 510(k) number K883112. 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 DERMATRON SKIN RESISTANCE METER?

DERMATRON SKIN RESISTANCE METER is a medical device that received FDA 510(k) clearance on 1989-08-10. The listed applicant is Raymar Electronics. The 510(k) number is K883112.

When did DERMATRON SKIN RESISTANCE METER receive FDA 510(k) clearance?

DERMATRON SKIN RESISTANCE METER received FDA 510(k) clearance on 1989-08-10, under 510(k) number K883112.

Who is the listed applicant for DERMATRON SKIN RESISTANCE METER?

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

What is the FDA product code for DERMATRON SKIN RESISTANCE METER?

The FDA product code for DERMATRON SKIN RESISTANCE 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

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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