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FDA 510(k)

NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL

K-Number: K030784 · 2004-04-01

Decision Date2004-04-01
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL is the device name listed in this FDA 510(k) record. The listed applicant is Applied Medical Technology, Inc.. It received FDA 510(k) clearance on 2004-04-01 under 510(k) number K030784. 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 NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL?

NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL is a medical device that received FDA 510(k) clearance on 2004-04-01. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K030784.

When did NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL receive FDA 510(k) clearance?

NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL received FDA 510(k) clearance on 2004-04-01, under 510(k) number K030784.

Who is the listed applicant for NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL?

The FDA 510(k) record lists Applied Medical Technology, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL?

The FDA product code for NASOGASTRIC BRIDLE SYSTEM WITH MAGNETIC RETRIEVAL 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 Technology, 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.

View all 21 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

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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