Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection
K-Number: K213174 · 2022-05-19
Device Summary
Frequently Asked Questions
What is the Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection?
Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection is a medical device that received FDA 510(k) clearance on 2022-05-19. The listed applicant is Cardinalhealth. The 510(k) number is K213174.
When did Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection receive FDA 510(k) clearance?
Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection received FDA 510(k) clearance on 2022-05-19, under 510(k) number K213174.
Who is the listed applicant for Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection?
The FDA 510(k) record lists Cardinalhealth as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection?
The FDA product code for Salem Sump Silicone Dual Lumen Stomach Tube with ENFit Connection is PIF.
Other records listing Cardinalhealth as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: PIF)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.