HILL NASOGASTRIC TUBE
K-Number: K883319 · 1988-12-05
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Device Summary
Frequently Asked Questions
What is the HILL NASOGASTRIC TUBE?
HILL NASOGASTRIC TUBE is a medical device that received FDA 510(k) clearance on 1988-12-05. The listed applicant is Zinetics Medical, Inc.. The 510(k) number is K883319.
When did HILL NASOGASTRIC TUBE receive FDA 510(k) clearance?
HILL NASOGASTRIC TUBE received FDA 510(k) clearance on 1988-12-05, under 510(k) number K883319.
Who is the listed applicant for HILL NASOGASTRIC TUBE?
The FDA 510(k) record lists Zinetics Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HILL NASOGASTRIC TUBE?
The FDA product code for HILL NASOGASTRIC TUBE is KNT.
Related Clinical Trials
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.
Other records listing Zinetics Medical, Inc. 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: KNT)
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.
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