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FDA 510(k)

PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES

K-Number: K972478 · 1998-02-09

Decision Date1998-02-09
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PRE-LOADED REPLACEMENT G-TUBES AND ACCESSORIES is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technologies. It received FDA 510(k) clearance on 1998-02-09 under 510(k) number K972478. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 23 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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