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FDA 510(k)

UR/RITE SYSTEM

K-Number: K833666 · 1984-01-13

ApplicantWright Laboratories, Inc.
Decision Date1984-01-13
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

UR/RITE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Wright Laboratories, Inc.. It received FDA 510(k) clearance on 1984-01-13 under 510(k) number K833666. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the UR/RITE SYSTEM?

UR/RITE SYSTEM is a medical device that received FDA 510(k) clearance on 1984-01-13. The listed applicant is Wright Laboratories, Inc.. The 510(k) number is K833666.

When did UR/RITE SYSTEM receive FDA 510(k) clearance?

UR/RITE SYSTEM received FDA 510(k) clearance on 1984-01-13, under 510(k) number K833666.

Who is the listed applicant for UR/RITE SYSTEM?

The FDA 510(k) record lists Wright Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UR/RITE SYSTEM?

The FDA product code for UR/RITE SYSTEM is JQW.

Related Clinical Trials

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Related Devices (Code: JQW)

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.

K023955BD VIPER INSTRUMENTBecton, Dickinson & COK973335QUATRO SP SAMPLE PROCESSING SYSTEMS (200-499, INCLUSIVE)Zenyx Scientific , Ltd.K9801802700 SAMPLE MANAGERWaters CorporationK970420MASTERCAP AM 5.0/MASTERCAP RM 5.0Pharmacia, Inc.K970616MINI SAMPLER PROCESSORCavro Scientific Instruments, Inc.K962687GIO. DE VITA E C. S.R.L.(GDV) AUTOMATIC WASHING SYSTEMNichols Institute Diagnostics

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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