TUBE, GASTRO-ENTEROSTOMY— 510(k) K760810

Name: FDA 510(k) clearance K760810
Creator: U.S. Food and Drug Administration
Published: 1977-02-28

Substantially Equivalent

Sherwood Medical Industries

FDA 510(k) clearance K760810 for TUBE, GASTRO-ENTEROSTOMY, Substantially Equivalent on 1977-02-28. Applicant: Sherwood Medical Industries. Device class: 2.

Clearance details

Applicant: Sherwood Medical Industries
Product code: Code EXD
Device class: Class 2
Regulation: 21 CFR 876.5895
Advisory panel: Gastroenterology, Urology
Date received: 1976-10-02
Decision date: 1977-02-28
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

Download summary PDF View on FDA.gov ↗

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