NON-IV ADAPTER FOR INFANT NG TUBE
K-Number: K072756 · 2007-12-19
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Device Summary
Frequently Asked Questions
What is the NON-IV ADAPTER FOR INFANT NG TUBE?
NON-IV ADAPTER FOR INFANT NG TUBE is a medical device that received FDA 510(k) clearance on 2007-12-19. The listed applicant is Promedic, Inc.. The 510(k) number is K072756.
When did NON-IV ADAPTER FOR INFANT NG TUBE receive FDA 510(k) clearance?
NON-IV ADAPTER FOR INFANT NG TUBE received FDA 510(k) clearance on 2007-12-19, under 510(k) number K072756.
Who is the listed applicant for NON-IV ADAPTER FOR INFANT NG TUBE?
The FDA 510(k) record lists Promedic, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for NON-IV ADAPTER FOR INFANT NG TUBE?
The FDA product code for NON-IV ADAPTER FOR INFANT NG 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 Promedic, 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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