FDA 510(k)

VANSONNENBERG GASTROSTOMY CATHETER

K-Number: K924850 · 1994-12-29

Decision Date1994-12-29

Product CodeKNT

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

VANSONNENBERG GASTROSTOMY CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corp. It received FDA 510(k) clearance on 1994-12-29 under 510(k) number K924850. 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 VANSONNENBERG GASTROSTOMY CATHETER?

VANSONNENBERG GASTROSTOMY CATHETER is a medical device that received FDA 510(k) clearance on 1994-12-29. The listed applicant is Boston Scientific Corp. The 510(k) number is K924850.

When did VANSONNENBERG GASTROSTOMY CATHETER receive FDA 510(k) clearance?

VANSONNENBERG GASTROSTOMY CATHETER received FDA 510(k) clearance on 1994-12-29, under 510(k) number K924850.

Who is the listed applicant for VANSONNENBERG GASTROSTOMY CATHETER?

The FDA 510(k) record lists Boston Scientific Corp as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VANSONNENBERG GASTROSTOMY CATHETER?

The FDA product code for VANSONNENBERG GASTROSTOMY CATHETER is KNT.

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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.