PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES
K-Number: K972478 · 1998-02-09
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Device Summary
Frequently Asked Questions
What is the PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES?
PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES is a medical device that received FDA 510(k) clearance on 1998-02-09. The listed applicant is Applied Medical Technologies. The 510(k) number is K972478.
When did PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES receive FDA 510(k) clearance?
PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES received FDA 510(k) clearance on 1998-02-09, under 510(k) number K972478.
Who is the listed applicant for PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES?
The FDA 510(k) record lists Applied Medical Technologies as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES?
The FDA product code for PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES 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 Applied Medical Technologies 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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