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FDA 510(k)

THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT

K-Number: K072476 · 2007-12-14

ApplicantBoston Scientific Corporation
Decision Date2007-12-14
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT is the device name listed in this FDA 510(k) record. The listed applicant is Boston Scientific Corporation. It received FDA 510(k) clearance on 2007-12-14 under 510(k) number K072476. 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 THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT?

THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT is a medical device that received FDA 510(k) clearance on 2007-12-14. The listed applicant is Boston Scientific Corporation. The 510(k) number is K072476.

When did THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT receive FDA 510(k) clearance?

THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT received FDA 510(k) clearance on 2007-12-14, under 510(k) number K072476.

Who is the listed applicant for THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT?

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

What is the FDA product code for THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT?

The FDA product code for THROUGH-THE-PEG (TTP) JEJUNOSTOMY TUBE KIT 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.

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