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FDA 510(k)

RUB E-Z

K-Number: K854396 · 1986-05-08

ApplicantE-Z Instruments Co.
Decision Date1986-05-08
Product CodeGYA
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

RUB E-Z is the device name listed in this FDA 510(k) record. The listed applicant is E-Z Instruments Co.. It received FDA 510(k) clearance on 1986-05-08 under 510(k) number K854396. The device is classified under product code GYA. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RUB E-Z?

RUB E-Z is a medical device that received FDA 510(k) clearance on 1986-05-08. The listed applicant is E-Z Instruments Co.. The 510(k) number is K854396.

When did RUB E-Z receive FDA 510(k) clearance?

RUB E-Z received FDA 510(k) clearance on 1986-05-08, under 510(k) number K854396.

Who is the listed applicant for RUB E-Z?

The FDA 510(k) record lists E-Z Instruments Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RUB E-Z?

The FDA product code for RUB E-Z is GYA.

Related Devices (Code: GYA)

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.

K883869DERMTRODEWorld Precision Instruments, Inc.K830877AP-CHECKGeneral DevicesK820040SC-IT IMPEDANCE TESTERCadwell Laboratories, Inc.K781475ELECTRODE IMPEDANCE TESTER-MODEL 500Life-Tech Instruments, 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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