FDA 510(k)

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY

K-Number: K924306 · 1995-05-15

ApplicantUnited States Endoscopy Group, Inc.

Decision Date1995-05-15

Product CodeKNT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY is the device name listed in this FDA 510(k) record. The listed applicant is United States Endoscopy Group, Inc.. It received FDA 510(k) clearance on 1995-05-15 under 510(k) number K924306. 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 PERCUTANEOUS ENDOSCOPIC GASTROSTOMY?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY is a medical device that received FDA 510(k) clearance on 1995-05-15. The listed applicant is United States Endoscopy Group, Inc.. The 510(k) number is K924306.

When did PERCUTANEOUS ENDOSCOPIC GASTROSTOMY receive FDA 510(k) clearance?

PERCUTANEOUS ENDOSCOPIC GASTROSTOMY received FDA 510(k) clearance on 1995-05-15, under 510(k) number K924306.

Who is the listed applicant for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY?

The FDA 510(k) record lists United States Endoscopy Group, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY?

The FDA product code for PERCUTANEOUS ENDOSCOPIC GASTROSTOMY is KNT.

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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.