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FDA 510(k)

DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER

K-Number: K960176 · 1996-07-24

ApplicantC.R. Bard, Inc.
Decision Date1996-07-24
Product CodeFEG
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER is the device name listed in this FDA 510(k) record. The listed applicant is C.R. Bard, Inc.. It received FDA 510(k) clearance on 1996-07-24 under 510(k) number K960176. The device is classified under product code FEG. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER?

DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER is a medical device that received FDA 510(k) clearance on 1996-07-24. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K960176.

When did DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER receive FDA 510(k) clearance?

DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER received FDA 510(k) clearance on 1996-07-24, under 510(k) number K960176.

Who is the listed applicant for DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER?

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

What is the FDA product code for DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER?

The FDA product code for DAVOL NASOGASTRIC SUMP TUBE W/PREVENT FILTER is FEG.

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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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