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)

HEMOGLOBIN ELECTROPHORESIS METH ON THE-

K-Number: K831055 · 1983-06-08

ApplicantOlympus Corp.
Decision Date1983-06-08
Product CodeJBO
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

HEMOGLOBIN ELECTROPHORESIS METH ON THE- is the device name listed in this FDA 510(k) record. The listed applicant is Olympus Corp.. It received FDA 510(k) clearance on 1983-06-08 under 510(k) number K831055. The device is classified under product code JBO. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HEMOGLOBIN ELECTROPHORESIS METH ON THE-?

HEMOGLOBIN ELECTROPHORESIS METH ON THE- is a medical device that received FDA 510(k) clearance on 1983-06-08. The listed applicant is Olympus Corp.. The 510(k) number is K831055.

When did HEMOGLOBIN ELECTROPHORESIS METH ON THE- receive FDA 510(k) clearance?

HEMOGLOBIN ELECTROPHORESIS METH ON THE- received FDA 510(k) clearance on 1983-06-08, under 510(k) number K831055.

Who is the listed applicant for HEMOGLOBIN ELECTROPHORESIS METH ON THE-?

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

What is the FDA product code for HEMOGLOBIN ELECTROPHORESIS METH ON THE-?

The FDA product code for HEMOGLOBIN ELECTROPHORESIS METH ON THE- is JBO.

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 Olympus Corp. 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.

K915402EW-10 AND EW-20K933200OLYMPUS PBD STENTSK942338OLYMPUS PF-8P OES PANCREATO FIBERSCOPE AND ACCESSORIESK931763HF-RESECTION ELECTRODE, LOOP W/RUNNER ENDOS/ACCESSK934835FLOVALK931764HF RESECTION ELECTRODE, LOOP W/RUNNER HYSTER/ACCES

View all 142 devices →

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.

↑