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FDA 510(k)

GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG

K-Number: K891371 · 1989-08-03

ApplicantEntech, Inc.
Decision Date1989-08-03
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG is the device name listed in this FDA 510(k) record. The listed applicant is Entech, Inc.. It received FDA 510(k) clearance on 1989-08-03 under 510(k) number K891371. 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 GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG?

GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG is a medical device that received FDA 510(k) clearance on 1989-08-03. The listed applicant is Entech, Inc.. The 510(k) number is K891371.

When did GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG receive FDA 510(k) clearance?

GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG received FDA 510(k) clearance on 1989-08-03, under 510(k) number K891371.

Who is the listed applicant for GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG?

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

What is the FDA product code for GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG?

The FDA product code for GILSDORF PERCU. ENDO.-PEG & PERCU. FLOURO.-PFG is KNT.

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Related Devices (Code: 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.

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