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FDA 510(k)

BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM

K-Number: K102391 · 2010-12-22

ApplicantC.R. Bard, Inc.
Decision Date2010-12-22
Product CodeKNT
Advisory CommitteeGU
DecisionUnknown

Device Summary

BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM 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 2010-12-22 under 510(k) number K102391. 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 BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM?

BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2010-12-22. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K102391.

When did BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM receive FDA 510(k) clearance?

BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM received FDA 510(k) clearance on 2010-12-22, under 510(k) number K102391.

Who is the listed applicant for BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM?

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 BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM?

The FDA product code for BARD DIGNISHIELD STOOL MANAGEMENT SYSTEM 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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