Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

SYSTEM 6000 AUTOMATED RIA ANALYZER

K-Number: K780886 · 1978-09-01

ApplicantBeckman Instruments, Inc.
Decision Date1978-09-01
Product CodeLCI
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYSTEM 6000 AUTOMATED RIA ANALYZER is the device name listed in this FDA 510(k) record. The listed applicant is Beckman Instruments, Inc.. It received FDA 510(k) clearance on 1978-09-01 under 510(k) number K780886. The device is classified under product code LCI. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYSTEM 6000 AUTOMATED RIA ANALYZER?

SYSTEM 6000 AUTOMATED RIA ANALYZER is a medical device that received FDA 510(k) clearance on 1978-09-01. The listed applicant is Beckman Instruments, Inc.. The 510(k) number is K780886.

When did SYSTEM 6000 AUTOMATED RIA ANALYZER receive FDA 510(k) clearance?

SYSTEM 6000 AUTOMATED RIA ANALYZER received FDA 510(k) clearance on 1978-09-01, under 510(k) number K780886.

Who is the listed applicant for SYSTEM 6000 AUTOMATED RIA ANALYZER?

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

What is the FDA product code for SYSTEM 6000 AUTOMATED RIA ANALYZER?

The FDA product code for SYSTEM 6000 AUTOMATED RIA ANALYZER is LCI.

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 Beckman 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.

K973448ACCESS TOXOPLASMA IGM REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER, MODELS 34460, 34465, 34469K982250ACCESS FREE T4 REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZERK981403IMMAGE IMMUNOCHEMISTRY SYSTEM VALPROIC ACID (VPA) REAGENTK981354ACCESS AFP REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER MODEL NUMBER 33211K980173ACCESS TOTAL BHCG REAGENTS ON THE ACCESS IMMUNOASSAY ANALYZER; 33500, 33505K974816ACCESS(R) PSA REAGENTS ON THE ACCESS(R) IMMUNOASSAY ANALYZER 33220, 33225, 33229

View all 281 devices →

Related Devices (Code: LCI)

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.

K98361725-HYDROXYVITAMIN D 125I RIA KITDiaSorin, Inc.K801037CENTRIA SYSTEM 2 AUTOMATED METHOD/RIAUnion Carbide Corp.

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.

↑