METRICARE ENTERAL FEEDING SYSTEM— 510(k) K895923

Name: FDA 510(k) clearance K895923
Creator: U.S. Food and Drug Administration
Published: 1990-07-19

Substantially Equivalent

Metrix Co.

FDA 510(k) clearance K895923 for METRICARE ENTERAL FEEDING SYSTEM, Substantially Equivalent on 1990-07-19. Applicant: Metrix Co.. Device class: 2.

Clearance details

Applicant: Metrix Co.
Product code: Code FPD
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1989-10-11
Decision date: 1990-07-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Dubuque, IA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Metrix Co.

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K030888 — EVA EMPTY SOLUTION CONTAINER2003-04-02
K895922 — METRICARE EMPTY CONTAINER SYSTEMS1990-08-22
K895924 — METRICARE DRUG RESERVOIRS1990-07-26
K761201 — ECHO-CARDIOTRACE, AUTOMATIC1977-01-12

Adverse events under product code FPD

product code FPD

Death: 6
Other: 1
Total: 7

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.