BARD DIGNICARE STOOL MANAGEMENT SYSTEM
K-Number: K073598 · 2008-06-13
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Device Summary
Frequently Asked Questions
What is the BARD DIGNICARE STOOL MANAGEMENT SYSTEM?
BARD DIGNICARE STOOL MANAGEMENT SYSTEM is a medical device that received FDA 510(k) clearance on 2008-06-13. The listed applicant is C.R. Bard, Inc.. The 510(k) number is K073598.
When did BARD DIGNICARE STOOL MANAGEMENT SYSTEM receive FDA 510(k) clearance?
BARD DIGNICARE STOOL MANAGEMENT SYSTEM received FDA 510(k) clearance on 2008-06-13, under 510(k) number K073598.
Who is the listed applicant for BARD DIGNICARE 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 DIGNICARE STOOL MANAGEMENT SYSTEM?
The FDA product code for BARD DIGNICARE STOOL MANAGEMENT SYSTEM is KNT.
Related Clinical Trials
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Other records listing C.R. Bard, Inc. as applicant
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
Related Devices (Code: KNT)
Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.
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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