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FDA 510(k)

RIA SOFTWARE

K-Number: K832760 · 1983-10-14

ApplicantKemble Instruments, Inc.
Decision Date1983-10-14
Product CodeJQP
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

RIA SOFTWARE is the device name listed in this FDA 510(k) record. The listed applicant is Kemble Instruments, Inc.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832760. The device is classified under product code JQP. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RIA SOFTWARE?

RIA SOFTWARE is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Kemble Instruments, Inc.. The 510(k) number is K832760.

When did RIA SOFTWARE receive FDA 510(k) clearance?

RIA SOFTWARE received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832760.

Who is the listed applicant for RIA SOFTWARE?

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

What is the FDA product code for RIA SOFTWARE?

The FDA product code for RIA SOFTWARE is JQP.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kemble Instruments, Inc. as applicant

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.

K842894KEMBLE 405K832734KEMTEK 400 RIA GAMMA COUNTERK832735KEMTEK 103 RIA GAMMA COUNTERK832736KEMTEK 104 RIA GAMMA COUNTERK830751KEMTEK 102K822293IMMU-COUNT 404

View all 9 devices →

Related Devices (Code: JQP)

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.

K113007BIONIME DIABETES MANAGEMENT SYSTEM VI.0Bionime CorporationK983468FASTTAKE ADAPTER, MODEL # P/N 020-072-01Selfcare, Inc.K964460THE ROBOLITEShai Syg Motion and Innovations, Ltd.K953652PRENVAL IBase Ten Systems, Inc.K934111MR7000 WITH TIME MANAGER SOFTWARE (TMS)Dynatech Laboratories, Inc.K923316EXPRESSO CARTRIDGEBio-Rad Laboratories, 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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