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FDA 510(k)

AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419)

K-Number: K073034 · 2008-03-14

Decision Date2008-03-14
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419) 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 2008-03-14 under 510(k) number K073034. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419)?

AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419) is a medical device that received FDA 510(k) clearance on 2008-03-14. The listed applicant is Applied Medical Technology, Inc.. The 510(k) number is K073034.

When did AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419) receive FDA 510(k) clearance?

AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419) received FDA 510(k) clearance on 2008-03-14, under 510(k) number K073034.

Who is the listed applicant for AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419)?

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 AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419)?

The FDA product code for AMT INITIAL PLACEMENT GI KIT (E2418) AND AMT DILATOR SET (E2419) 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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