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)

ANALYZER, AUTOMED CENTRIFUGAL

K-Number: K781900 · 1978-12-20

ApplicantAutogenic Systems
Decision Date1978-12-20
Product CodeJJG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ANALYZER, AUTOMED CENTRIFUGAL is the device name listed in this FDA 510(k) record. The listed applicant is Autogenic Systems. It received FDA 510(k) clearance on 1978-12-20 under 510(k) number K781900. The device is classified under product code JJG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANALYZER, AUTOMED CENTRIFUGAL?

ANALYZER, AUTOMED CENTRIFUGAL is a medical device that received FDA 510(k) clearance on 1978-12-20. The listed applicant is Autogenic Systems. The 510(k) number is K781900.

When did ANALYZER, AUTOMED CENTRIFUGAL receive FDA 510(k) clearance?

ANALYZER, AUTOMED CENTRIFUGAL received FDA 510(k) clearance on 1978-12-20, under 510(k) number K781900.

Who is the listed applicant for ANALYZER, AUTOMED CENTRIFUGAL?

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

What is the FDA product code for ANALYZER, AUTOMED CENTRIFUGAL?

The FDA product code for ANALYZER, AUTOMED CENTRIFUGAL is JJG.

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

Related Devices (Code: JJG)

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.

K972409AG CHEMISTRY ANALYZER SYSTEMLandmark Scientific, Inc.K942782PICCOLO(TM)Abaxis, Inc.K934592EPOC 2000 POINT-OF-CARE ANALYZER AND EPOC 5-CHEMISTRY REAGENT ROTORAbaxis, Inc.K920942OLYMPUS AU800 CLINICAL CHEMISTRY ANALYZEROlympus Corp.K910222COBAS ALPHARoche Diagnostic Systems, Inc.K903626BIOMEK AUTOMATED LABORATORY WORKSTATION W/GENELISABeckman 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.

↑