FDA 510(k)

HDL CHOLESTEROL-E

K-Number: K863065 · 1986-09-25

Decision Date1986-09-25

Product Code

DecisionSubstantially Equivalent

Device Summary

HDL CHOLESTEROL-E is the device name listed in this FDA 510(k) record. The listed applicant is J. D. Assoc.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K863065. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HDL CHOLESTEROL-E?

HDL CHOLESTEROL-E is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is J. D. Assoc.. The 510(k) number is K863065.

When did HDL CHOLESTEROL-E receive FDA 510(k) clearance?

HDL CHOLESTEROL-E received FDA 510(k) clearance on 1986-09-25, under 510(k) number K863065.

Who is the listed applicant for HDL CHOLESTEROL-E?

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

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing J. D. Assoc. as applicant

K863054AST S.C.E. (GOT)K863103PEG 6,000 K863069MAGNESIOMETER K863079CREATINKINETIC K863068LDH S.C.E.K863112PROTEINMETER

View all 34 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.