MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT— 510(k) K844850

Name: FDA 510(k) clearance K844850
Creator: U.S. Food and Drug Administration
Published: 1985-04-02

Substantially Equivalent

Medicorp, Inc.

FDA 510(k) clearance K844850 for MEDICORP DEHYDRACON A DEHYDRATED DIALYSATE CONCENT, Substantially Equivalent on 1985-04-02. Applicant: Medicorp, Inc.. Device class: 2.

Clearance details

Applicant: Medicorp, Inc.
Product code: Code FKQ
Device class: Class 2
Regulation: 21 CFR 876.5820
Advisory panel: Gastroenterology, Urology
Date received: 1984-12-13
Decision date: 1985-04-02
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Salt Lake City, UT, US

Download summary PDF View on FDA.gov ↗

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Adverse events under product code FKQ

product code FKQ

Other: 1
Total: 1

Source: openFDA MAUDE database, 2020-01-01 through 2026-04-23. Counts aggregate all devices under this product code, not just this specific clearance. Reports are submissions to FDA, not validated events. Search MAUDE directly →

Data sourced from openFDA. This site is unofficial and independent of the FDA.