TurboSEAL Nasogastric Aspiration Tube— 510(k) K142483

Name: FDA 510(k) clearance K142483
Creator: U.S. Food and Drug Administration
Published: 2014-12-19

Substantially Equivalent

Turboseal, L.P.

FDA 510(k) clearance K142483 for TurboSEAL Nasogastric Aspiration Tube, Substantially Equivalent on 2014-12-19. Applicant: Turboseal, L.P.. Device class: 2.

Clearance details

Applicant: Turboseal, L.P.
Product code: Code BSS
Device class: Class 2
Regulation: 21 CFR 876.5980
Advisory panel: Gastroenterology, Urology
Date received: 2014-09-04
Decision date: 2014-12-19
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Tel Aviv, IL

Download summary PDF View on FDA.gov ↗

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