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FDA 510(k)

GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY

K-Number: K923488 · 1995-07-20

Decision Date1995-07-20
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY 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 1995-07-20 under 510(k) number K923488. 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 GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY?

GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY is a medical device that received FDA 510(k) clearance on 1995-07-20. The listed applicant is Applied Medical Technologies. The 510(k) number is K923488.

When did GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY receive FDA 510(k) clearance?

GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY received FDA 510(k) clearance on 1995-07-20, under 510(k) number K923488.

Who is the listed applicant for GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY?

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 GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY?

The FDA product code for GASTRANIMAL PERCUTANEOUS REPLACEMENT GASTROOMY 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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