TUBE, FEEDING, ARGYLE— 510(k) K760137

Name: FDA 510(k) clearance K760137
Creator: U.S. Food and Drug Administration
Published: 1976-07-16

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760137 for TUBE, FEEDING, ARGYLE, Substantially Equivalent on 1976-07-16. Applicant: Sherwood Medical Industries. Device class: 2.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code FPD
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 1976-06-28
Decision date: 1976-07-16
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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K792013 — LANCER L-INA HUMAN REFERENCE SERUM1979-11-13
K792014 — LANCER L-INA BUFFER, POLYMER, WASH SOLU1979-11-13
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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.